Canonical Allele Identifier: CA1242199336
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533677A= , CM000664.2:g.31533677A= GRCh38
NC_000002.11:g.31758747A= , CM000664.1:g.31758747A= GRCh37
NC_000002.10:g.31612251A= NCBI36
NG_008365.1:g.52295T=

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.371T= MANE Select ENSP00000477587.1:p.Val124=
ENST00000622030.1:c.371T= ENSP00000477587.1:p.Val124=
NM_000348.3:c.371T= NP_000339.2:p.Val124=
XM_011533068.1:c.371T= XP_011531370.1:p.Val124=
XM_011533069.1:c.149T= XP_011531371.1:p.Val50=
XM_011533070.1:c.116T= XP_011531372.1:p.Val39=
XM_011533071.1:c.116T= XP_011531373.1:p.Val39=
XM_011533072.1:c.116T= XP_011531374.1:p.Val39=
XM_011533069.2:c.149T= XP_011531371.1:p.Val50=
XM_011533072.2:c.116T= XP_011531374.1:p.Val39=
NM_000348.4:c.371T= MANE Select NP_000339.2:p.Val124=