Canonical Allele Identifier: CA1242197378

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529335G= , CM000664.2:g.31529335G=	GRCh38
NC_000002.11:g.31754405G= , CM000664.1:g.31754405G=	GRCh37
NC_000002.10:g.31607909G=	NCBI36
NG_008365.1:g.56637C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.670C= MANE Select	ENSP00000477587.1:p.Leu224=
ENST00000622030.1:c.670C=	ENSP00000477587.1:p.Leu224=
NM_000348.3:c.670C=	NP_000339.2:p.Leu224=
XM_011533069.1:c.448C=	XP_011531371.1:p.Leu150=
XM_011533070.1:c.415C=	XP_011531372.1:p.Leu139=
XM_011533071.1:c.415C=	XP_011531373.1:p.Leu139=
XM_011533072.1:c.415C=	XP_011531374.1:p.Leu139=
XM_011533069.2:c.448C=	XP_011531371.1:p.Leu150=
XM_011533072.2:c.415C=	XP_011531374.1:p.Leu139=
NM_000348.4:c.670C= MANE Select	NP_000339.2:p.Leu224=