Canonical Allele Identifier: CA1242199332
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533671T= , CM000664.2:g.31533671T= GRCh38
NC_000002.11:g.31758741T= , CM000664.1:g.31758741T= GRCh37
NC_000002.10:g.31612245T= NCBI36
NG_008365.1:g.52301A=

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.377A= MANE Select ENSP00000477587.1:p.Gln126=
ENST00000622030.1:c.377A= ENSP00000477587.1:p.Gln126=
NM_000348.3:c.377A= NP_000339.2:p.Gln126=
XM_011533068.1:c.377A= XP_011531370.1:p.Gln126=
XM_011533069.1:c.155A= XP_011531371.1:p.Gln52=
XM_011533070.1:c.122A= XP_011531372.1:p.Gln41=
XM_011533071.1:c.122A= XP_011531373.1:p.Gln41=
XM_011533072.1:c.122A= XP_011531374.1:p.Gln41=
XM_011533069.2:c.155A= XP_011531371.1:p.Gln52=
XM_011533072.2:c.122A= XP_011531374.1:p.Gln41=
NM_000348.4:c.377A= MANE Select NP_000339.2:p.Gln126=