Nucleotide

Homo sapiens isolate CHM13 chromosome X

Select item 20337172522.

154,259,566 bp linear DNA

Accession:: CP068255.2
GI:: 2033717252

Assembly BioProject BioSample PubMed Taxonomy

Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 3, mRNA

Select item 16751785173.

5,604 bp linear mRNA

Accession:: NM_001171689.2
GI:: 1675178517

Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 2, mRNA

Select item 16751763044.

5,239 bp linear mRNA

Accession:: NM_001025580.2
GI:: 1675176304

Homo sapiens AMMECR nuclear protein 1 (AMMECR1), RefSeqGene on chromosome X

Select item 15433837025.

253,048 bp linear DNA

Accession:: NG_016469.2
GI:: 1543383702

Protein Taxonomy

Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 1, mRNA

Select item 15192419306.

5,350 bp linear mRNA

Accession:: NM_015365.3
GI:: 1519241930

Homo sapiens Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1 isoform 2 (AMMECR1) mRNA, partial cds

Select item 9579506947.

999 bp linear mRNA

Accession:: KU178497.1
GI:: 957950694

Homo sapiens Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1 isoform 1 (AMMECR1) mRNA, partial cds

Select item 9579506908.

888 bp linear mRNA

Accession:: KU178496.1
GI:: 957950690

Homo sapiens chromosome X, GRCh38.p14 Primary Assembly

Select item 5688155759.

156,040,895 bp linear DNA

Accession:: NC_000023.11
GI:: 568815575

Assembly BioProject Protein PubMed Taxonomy

Homo sapiens chromosome X WGS contig WGS_FIN_AC000113.1_100190 genomic sequence

Select item 52746704710.

250 bp linear DNA

Accession:: KF459306.1
GI:: 527467047

Taxonomy

Homo sapiens cDNA, FLJ95432, highly similar to Homo sapiens Alport syndrome, mental retardation, midfacehypoplasia and elliptocytosis chromosomal region, gene 1 (AMMECR1),mRNA

Select item 16469834311.

1,014 bp linear mRNA

Accession:: AK314596.1
GI:: 164698343

Protein Taxonomy

DA203031 BRAWH2 Homo sapiens cDNA clone BRAWH2008483 5', mRNA sequence

Select item 7829141712.

532 bp linear mRNA

Accession:: DA203031.1
GI:: 78291417

BioSample PubMed Taxonomy

Homo sapiens 211000035842847 genomic scaffold, whole genome shotgun sequence

Select item 7423002513.

11,680,561 bp linear DNA

Accession:: CH471120.2
GI:: 74230025

Assembly BioProject BioSample Protein PubMed Taxonomy

Homo sapiens cDNA clone IMAGE:4748592, partial cds

Select item 4080721414.

1,380 bp linear mRNA

Accession:: BC065214.1
GI:: 40807214

Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1, mRNA (cDNA clone MGC:71655 IMAGE:30344824), complete cds

Select item 3851152515.

3,053 bp linear mRNA

Accession:: BC060813.1
GI:: 38511525

Homo sapiens mRNA; cDNA DKFZp686L16148 (from clone DKFZp686L16148)

Select item 3436796216.

3,065 bp linear mRNA

Accession:: BX648797.1
GI:: 34367962

Taxonomy

Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1, mRNA (cDNA clone IMAGE:6168870)

Select item 3035402217.

2,331 bp linear mRNA

Accession:: BC051895.1
GI:: 30354022

Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1, mRNA (cDNA clone IMAGE:5405764)

Select item 2327371618.

2,271 bp linear mRNA

Accession:: BC037983.1
GI:: 23273716

Homo sapiens cDNA FLJ34111 fis, clone FCBBF3008748, highly similar to AMME syndrome candidate gene 1 protein homolog

Select item 2174980019.

3,381 bp linear mRNA

Accession:: AK091430.1
GI:: 21749800

Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1, mRNA (cDNA clone IMAGE:5140448)

Select item 1935411820.

942 bp linear mRNA

Accession:: BC024762.1
GI:: 19354118