Canonical Allele Identifier: CA1242198189

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531134G= , CM000664.2:g.31531134G=	GRCh38
NC_000002.11:g.31756204G= , CM000664.1:g.31756204G=	GRCh37
NC_000002.10:g.31609708G=	NCBI36
NG_008365.1:g.54838C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.547+237C= MANE Select	ENSP00000477587.1:n.547+237C=
ENST00000622030.1:c.547+237C=	ENSP00000477587.1:n.547+237C=
NM_000348.3:c.547+237C=	NP_000339.2:n.547+237C=
XM_011533069.1:c.325+237C=	XP_011531371.1:n.325+237C=
XM_011533070.1:c.292+237C=	XP_011531372.1:n.292+237C=
XM_011533071.1:c.292+237C=	XP_011531373.1:n.292+237C=
XM_011533072.1:c.292+237C=	XP_011531374.1:n.292+237C=
XM_011533069.2:c.325+237C=	XP_011531371.1:n.325+237C=
XM_011533072.2:c.292+237C=	XP_011531374.1:n.292+237C=
NM_000348.4:c.547+237C= MANE Select	NP_000339.2:n.547+237C=