Canonical Allele Identifier: CA2004808869

Gene: SC5D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121303426G= , CM000673.2:g.121303426G=	GRCh38
NC_000011.9:g.121174135G= , CM000673.1:g.121174135G=	GRCh37
NC_000011.8:g.120679345G=	NCBI36
NG_009446.1:g.15748G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.51G= MANE Select	ENSP00000264027.4:p.Val17=
ENST00000264027.8:c.51G=	ENSP00000264027.4:p.Val17=
ENST00000392789.2:c.51G=	ENSP00000376539.2:p.Val17=
ENST00000524683.5:n.107G=
ENST00000527762.5:c.51G=	ENSP00000436290.1:p.Val17=
ENST00000531140.1:n.119G=
ENST00000534230.5:c.51G=	ENSP00000432550.1:p.Val17=
ENST00000534455.5:n.197G=
NM_001024956.2:c.51G=	NP_001020127.1:p.Val17=
NM_006918.4:c.51G=	NP_008849.2:p.Val17=
NM_006918.5:c.51G= MANE Select	NP_008849.2:p.Val17=
NM_001024956.3:c.51G=	NP_001020127.1:p.Val17=