Canonical Allele Identifier: CA1242198233

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531219A= , CM000664.2:g.31531219A=	GRCh38
NC_000002.11:g.31756289A= , CM000664.1:g.31756289A=	GRCh37
NC_000002.10:g.31609793A=	NCBI36
NG_008365.1:g.54753T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.547+152T= MANE Select	ENSP00000477587.1:n.547+152T=
ENST00000622030.1:c.547+152T=	ENSP00000477587.1:n.547+152T=
NM_000348.3:c.547+152T=	NP_000339.2:n.547+152T=
XM_011533069.1:c.325+152T=	XP_011531371.1:n.325+152T=
XM_011533070.1:c.292+152T=	XP_011531372.1:n.292+152T=
XM_011533071.1:c.292+152T=	XP_011531373.1:n.292+152T=
XM_011533072.1:c.292+152T=	XP_011531374.1:n.292+152T=
XM_011533069.2:c.325+152T=	XP_011531371.1:n.325+152T=
XM_011533072.2:c.292+152T=	XP_011531374.1:n.292+152T=
NM_000348.4:c.547+152T= MANE Select	NP_000339.2:n.547+152T=