Canonical Allele Identifier: CA1242196081

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526548A= , CM000664.2:g.31526548A=	GRCh38
NC_000002.11:g.31751618A= , CM000664.1:g.31751618A=	GRCh37
NC_000002.10:g.31605122A=	NCBI36
NG_008365.1:g.59424T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-286T= MANE Select	ENSP00000477587.1:n.699-286T=
ENST00000622030.1:c.699-286T=	ENSP00000477587.1:n.699-286T=
NM_000348.3:c.699-286T=	NP_000339.2:n.699-286T=
XM_011533069.1:c.477-286T=	XP_011531371.1:n.477-286T=
XM_011533070.1:c.444-286T=	XP_011531372.1:n.444-286T=
XM_011533071.1:c.444-286T=	XP_011531373.1:n.444-286T=
XM_011533072.1:c.444-286T=	XP_011531374.1:n.444-286T=
XM_011533069.2:c.477-286T=	XP_011531371.1:n.477-286T=
XM_011533072.2:c.444-286T=	XP_011531374.1:n.444-286T=
NM_000348.4:c.699-286T= MANE Select	NP_000339.2:n.699-286T=