Canonical Allele Identifier: CA1459044898

Gene: SRD5A3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55346379C= , CM000666.2:g.55346379C=	GRCh38
NC_000004.11:g.56212546C= , CM000666.1:g.56212546C=	GRCh37
NC_000004.10:g.55907303C=	NCBI36
NG_028230.1:g.5159C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.43C= MANE Select	ENSP00000264228.4:p.Leu15=
ENST00000679351.1:c.43C=	ENSP00000505676.1:p.Leu15=
ENST00000679707.1:c.43C=	ENSP00000505713.1:p.Leu15=
ENST00000679836.1:c.43C=	ENSP00000506601.1:p.Leu15=
ENST00000680700.1:c.43C=	ENSP00000504926.1:p.Leu15=
ENST00000264228.8:c.43C=	ENSP00000264228.4:p.Leu15=
NM_024592.4:c.43C=	NP_078868.1:p.Leu15=
XM_005265766.2:c.43C=	XP_005265823.1:p.Leu15=
XM_005265767.2:c.43C=	XP_005265824.1:p.Leu15=
XM_005265766.4:c.43C=	XP_005265823.1:p.Leu15=
XM_005265767.3:c.43C=	XP_005265824.1:p.Leu15=
NM_024592.5:c.43C= MANE Select	NP_078868.1:p.Leu15=