Canonical Allele Identifier: CA1242198218

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531197T= , CM000664.2:g.31531197T=	GRCh38
NC_000002.11:g.31756267T= , CM000664.1:g.31756267T=	GRCh37
NC_000002.10:g.31609771T=	NCBI36
NG_008365.1:g.54775A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.547+174A= MANE Select	ENSP00000477587.1:n.547+174A=
ENST00000622030.1:c.547+174A=	ENSP00000477587.1:n.547+174A=
NM_000348.3:c.547+174A=	NP_000339.2:n.547+174A=
XM_011533069.1:c.325+174A=	XP_011531371.1:n.325+174A=
XM_011533070.1:c.292+174A=	XP_011531372.1:n.292+174A=
XM_011533071.1:c.292+174A=	XP_011531373.1:n.292+174A=
XM_011533072.1:c.292+174A=	XP_011531374.1:n.292+174A=
XM_011533069.2:c.325+174A=	XP_011531371.1:n.325+174A=
XM_011533072.2:c.292+174A=	XP_011531374.1:n.292+174A=
NM_000348.4:c.547+174A= MANE Select	NP_000339.2:n.547+174A=