Canonical Allele Identifier: CA1459051022

Gene: SRD5A3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359428G= , CM000666.2:g.55359428G=	GRCh38
NC_000004.11:g.56225595G= , CM000666.1:g.56225595G=	GRCh37
NC_000004.10:g.55920352G=	NCBI36
NG_028230.1:g.18208G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.304G= MANE Select	ENSP00000264228.4:p.Ala102=
ENST00000677177.2:c.17G=
ENST00000678717.1:n.201G=
ENST00000679351.1:c.304G=	ENSP00000505676.1:p.Ala102=
ENST00000679707.1:c.304G=	ENSP00000505713.1:p.Ala102=
ENST00000679836.1:c.304G=	ENSP00000506601.1:p.Ala102=
ENST00000680700.1:c.304G=	ENSP00000504926.1:p.Ala102=
ENST00000264228.8:c.304G=	ENSP00000264228.4:p.Ala102=
ENST00000505210.1:c.229G=	ENSP00000424714.1:p.Ala77=
ENST00000514398.1:n.313G=
NM_024592.4:c.304G=	NP_078868.1:p.Ala102=
XM_005265766.2:c.304G=	XP_005265823.1:p.Ala102=
XM_005265767.2:c.304G=	XP_005265824.1:p.Ala102=
XM_005265766.4:c.304G=	XP_005265823.1:p.Ala102=
XM_005265767.3:c.304G=	XP_005265824.1:p.Ala102=
XM_017008601.1:c.169G=	XP_016864090.1:p.Ala57=
NM_024592.5:c.304G= MANE Select	NP_078868.1:p.Ala102=