Canonical Allele Identifier: CA1242197426
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529439A= , CM000664.2:g.31529439A= GRCh38
NC_000002.11:g.31754509A= , CM000664.1:g.31754509A= GRCh37
NC_000002.10:g.31608013A= NCBI36
NG_008365.1:g.56533T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.566T= MANE Select ENSP00000477587.1:p.Val189=
ENST00000622030.1:c.566T= ENSP00000477587.1:p.Val189=
NM_000348.3:c.566T= NP_000339.2:p.Val189=
XM_011533069.1:c.344T= XP_011531371.1:p.Val115=
XM_011533070.1:c.311T= XP_011531372.1:p.Val104=
XM_011533071.1:c.311T= XP_011531373.1:p.Val104=
XM_011533072.1:c.311T= XP_011531374.1:p.Val104=
XM_011533069.2:c.344T= XP_011531371.1:p.Val115=
XM_011533072.2:c.311T= XP_011531374.1:p.Val104=
NM_000348.4:c.566T= MANE Select NP_000339.2:p.Val189=