Canonical Allele Identifier: CA1242199354
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533717G= , CM000664.2:g.31533717G= GRCh38
NC_000002.11:g.31758787G= , CM000664.1:g.31758787G= GRCh37
NC_000002.10:g.31612291G= NCBI36
NG_008365.1:g.52255C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.331C= MANE Select ENSP00000477587.1:p.Leu111=
ENST00000622030.1:c.331C= ENSP00000477587.1:p.Leu111=
NM_000348.3:c.331C= NP_000339.2:p.Leu111=
XM_011533068.1:c.331C= XP_011531370.1:p.Leu111=
XM_011533069.1:c.109C= XP_011531371.1:p.Leu37=
XM_011533070.1:c.76C= XP_011531372.1:p.Leu26=
XM_011533071.1:c.76C= XP_011531373.1:p.Leu26=
XM_011533072.1:c.76C= XP_011531374.1:p.Leu26=
XM_011533069.2:c.109C= XP_011531371.1:p.Leu37=
XM_011533072.2:c.76C= XP_011531374.1:p.Leu26=
NM_000348.4:c.331C= MANE Select NP_000339.2:p.Leu111=