Canonical Allele Identifier: CA1459051044

Gene: SRD5A3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359485C= , CM000666.2:g.55359485C=	GRCh38
NC_000004.11:g.56225652C= , CM000666.1:g.56225652C=	GRCh37
NC_000004.10:g.55920409C=	NCBI36
NG_028230.1:g.18265C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.361C= MANE Select	ENSP00000264228.4:p.Gln121=
ENST00000677177.2:c.74C=
ENST00000678717.1:n.258C=
ENST00000679351.1:c.361C=	ENSP00000505676.1:p.Gln121=
ENST00000679707.1:c.361C=	ENSP00000505713.1:p.Gln121=
ENST00000679836.1:c.361C=	ENSP00000506601.1:p.Gln121=
ENST00000680700.1:c.361C=	ENSP00000504926.1:p.Gln121=
ENST00000264228.8:c.361C=	ENSP00000264228.4:p.Gln121=
ENST00000505210.1:c.286C=	ENSP00000424714.1:p.Gln96=
ENST00000514398.1:n.370C=
NM_024592.4:c.361C=	NP_078868.1:p.Gln121=
XM_005265766.2:c.361C=	XP_005265823.1:p.Gln121=
XM_005265767.2:c.361C=	XP_005265824.1:p.Gln121=
XM_005265766.4:c.361C=	XP_005265823.1:p.Gln121=
XM_005265767.3:c.361C=	XP_005265824.1:p.Gln121=
XM_017008601.1:c.226C=	XP_016864090.1:p.Gln76=
NM_024592.5:c.361C= MANE Select	NP_078868.1:p.Gln121=