Canonical Allele Identifier: CA425568258
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533640G>A , CM000664.2:g.31533640G>A GRCh38
NC_000002.11:g.31758710G>A , CM000664.1:g.31758710G>A GRCh37
NC_000002.10:g.31612214G>A NCBI36
NG_008365.1:g.52332C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000348.4:c.408C>T MANE Select NP_000339.2:p.Tyr136=
ENST00000622030.2:c.408C>T MANE Select ENSP00000477587.1:p.Tyr136=
NM_000348.3:c.408C>T NP_000339.2:p.Tyr136=
ENST00000622030.1:c.408C>T ENSP00000477587.1:p.Tyr136=
XM_011533068.1:c.408C>T XP_011531370.1:p.Tyr136=
XM_011533069.1:c.186C>T XP_011531371.1:p.Tyr62=
XM_011533069.2:c.186C>T XP_011531371.1:p.Tyr62=
XM_011533070.1:c.153C>T XP_011531372.1:p.Tyr51=
XM_011533071.1:c.153C>T XP_011531373.1:p.Tyr51=
XM_011533072.1:c.153C>T XP_011531374.1:p.Tyr51=
XM_011533072.2:c.153C>T XP_011531374.1:p.Tyr51=