Canonical Allele Identifier: CA1459050996

Gene: SRD5A3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359361T= , CM000666.2:g.55359361T=	GRCh38
NC_000004.11:g.56225528T= , CM000666.1:g.56225528T=	GRCh37
NC_000004.10:g.55920285T=	NCBI36
NG_028230.1:g.18141T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.237T= MANE Select	ENSP00000264228.4:p.Phe79=
ENST00000678717.1:n.134T=
ENST00000679351.1:c.237T=	ENSP00000505676.1:p.Phe79=
ENST00000679707.1:c.237T=	ENSP00000505713.1:p.Phe79=
ENST00000679836.1:c.237T=	ENSP00000506601.1:p.Phe79=
ENST00000680700.1:c.237T=	ENSP00000504926.1:p.Phe79=
ENST00000264228.8:c.237T=	ENSP00000264228.4:p.Phe79=
ENST00000505210.1:c.162T=	ENSP00000424714.1:p.Phe54=
ENST00000514398.1:n.246T=
NM_024592.4:c.237T=	NP_078868.1:p.Phe79=
XM_005265766.2:c.237T=	XP_005265823.1:p.Phe79=
XM_005265767.2:c.237T=	XP_005265824.1:p.Phe79=
XM_005265766.4:c.237T=	XP_005265823.1:p.Phe79=
XM_005265767.3:c.237T=	XP_005265824.1:p.Phe79=
XM_017008601.1:c.102T=	XP_016864090.1:p.Phe34=
NM_024592.5:c.237T= MANE Select	NP_078868.1:p.Phe79=