Canonical Allele Identifier: CA2035390489
Gene: AQP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49950964C= , CM000674.2:g.49950964C= GRCh38
NC_000012.11:g.50344747C= , CM000674.1:g.50344747C= GRCh37
NC_000012.10:g.48631014C= NCBI36
NG_008913.1:g.5224C= , LRG_717:g.5224C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000199280.4:c.134C= MANE Select ENSP00000199280.3:p.Ala45=
ENST00000199280.3:c.134C= ENSP00000199280.3:p.Ala45=
ENST00000550862.1:c.134C= ENSP00000450022.1:p.Ala45=
ENST00000551526.5:c.134C= ENSP00000447148.1:p.Ala45=
NM_000486.5:c.134C= , LRG_717t1:c.134C= NP_000477.1:p.Ala45=
NM_000486.6:c.134C= MANE Select NP_000477.1:p.Ala45=