Canonical Allele Identifier: CA1242199317
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533628C= , CM000664.2:g.31533628C= GRCh38
NC_000002.11:g.31758698C= , CM000664.1:g.31758698C= GRCh37
NC_000002.10:g.31612202C= NCBI36
NG_008365.1:g.52344G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.420G= MANE Select ENSP00000477587.1:p.Trp140=
ENST00000622030.1:c.420G= ENSP00000477587.1:p.Trp140=
NM_000348.3:c.420G= NP_000339.2:p.Trp140=
XM_011533068.1:c.420G= XP_011531370.1:p.Trp140=
XM_011533069.1:c.198G= XP_011531371.1:p.Trp66=
XM_011533070.1:c.165G= XP_011531372.1:p.Trp55=
XM_011533071.1:c.165G= XP_011531373.1:p.Trp55=
XM_011533072.1:c.165G= XP_011531374.1:p.Trp55=
XM_011533069.2:c.198G= XP_011531371.1:p.Trp66=
XM_011533072.2:c.165G= XP_011531374.1:p.Trp55=
NM_000348.4:c.420G= MANE Select NP_000339.2:p.Trp140=