Canonical Allele Identifier: CA1242199335
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533676G= , CM000664.2:g.31533676G= GRCh38
NC_000002.11:g.31758746G= , CM000664.1:g.31758746G= GRCh37
NC_000002.10:g.31612250G= NCBI36
NG_008365.1:g.52296C=

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.372C= MANE Select ENSP00000477587.1:p.Val124=
ENST00000622030.1:c.372C= ENSP00000477587.1:p.Val124=
NM_000348.3:c.372C= NP_000339.2:p.Val124=
XM_011533068.1:c.372C= XP_011531370.1:p.Val124=
XM_011533069.1:c.150C= XP_011531371.1:p.Val50=
XM_011533070.1:c.117C= XP_011531372.1:p.Val39=
XM_011533071.1:c.117C= XP_011531373.1:p.Val39=
XM_011533072.1:c.117C= XP_011531374.1:p.Val39=
XM_011533069.2:c.150C= XP_011531371.1:p.Val50=
XM_011533072.2:c.117C= XP_011531374.1:p.Val39=
NM_000348.4:c.372C= MANE Select NP_000339.2:p.Val124=