Canonical Allele Identifier: CA1242199357
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533723C= , CM000664.2:g.31533723C= GRCh38
NC_000002.11:g.31758793C= , CM000664.1:g.31758793C= GRCh37
NC_000002.10:g.31612297C= NCBI36
NG_008365.1:g.52249G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.325G= MANE Select ENSP00000477587.1:p.Ala109=
ENST00000622030.1:c.325G= ENSP00000477587.1:p.Ala109=
NM_000348.3:c.325G= NP_000339.2:p.Ala109=
XM_011533068.1:c.325G= XP_011531370.1:p.Ala109=
XM_011533069.1:c.103G= XP_011531371.1:p.Ala35=
XM_011533070.1:c.70G= XP_011531372.1:p.Ala24=
XM_011533071.1:c.70G= XP_011531373.1:p.Ala24=
XM_011533072.1:c.70G= XP_011531374.1:p.Ala24=
XM_011533069.2:c.103G= XP_011531371.1:p.Ala35=
XM_011533072.2:c.70G= XP_011531374.1:p.Ala24=
NM_000348.4:c.325G= MANE Select NP_000339.2:p.Ala109=