Canonical Allele Identifier: CA5026458
Gene: AQP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33443438C>T , CM000671.2:g.33443438C>T GRCh38
NC_000009.11:g.33443436C>T , CM000671.1:g.33443436C>T GRCh37
NC_000009.10:g.33433436C>T NCBI36
NG_007476.1:g.9155G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297991.6:c.256G>A MANE Select ENSP00000297991.4:p.Val86Met
ENST00000643650.1:c.278G>A ENSP00000493567.1:p.Arg93His
ENST00000645858.1:c.256G>A ENSP00000493516.1:p.Val86Met
ENST00000297991.4:c.256G>A ENSP00000297991.4:p.Val86Met
ENST00000463983.5:n.308G>A
ENST00000473153.1:n.235G>A
ENST00000493581.1:n.629G>A
NM_004925.4:c.256G>A NP_004916.1:p.Val86Met
XM_011517864.1:c.256G>A XP_011516166.1:p.Val86Met
NM_001318144.1:c.256G>A NP_001305073.1:p.Val86Met
XR_001746289.1:n.322G>A
NM_004925.5:c.256G>A MANE Select NP_004916.1:p.Val86Met
NM_001318144.2:c.256G>A NP_001305073.1:p.Val86Met