Canonical Allele Identifier: CA2004808868

Gene: SC5D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121303425T= , CM000673.2:g.121303425T=	GRCh38
NC_000011.9:g.121174134T= , CM000673.1:g.121174134T=	GRCh37
NC_000011.8:g.120679344T=	NCBI36
NG_009446.1:g.15747T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264027.9:c.50T= MANE Select	ENSP00000264027.4:p.Val17=
ENST00000264027.8:c.50T=	ENSP00000264027.4:p.Val17=
ENST00000392789.2:c.50T=	ENSP00000376539.2:p.Val17=
ENST00000524683.5:n.106T=
ENST00000527762.5:c.50T=	ENSP00000436290.1:p.Val17=
ENST00000531140.1:n.118T=
ENST00000534230.5:c.50T=	ENSP00000432550.1:p.Val17=
ENST00000534455.5:n.196T=
NM_001024956.2:c.50T=	NP_001020127.1:p.Val17=
NM_006918.4:c.50T=	NP_008849.2:p.Val17=
NM_006918.5:c.50T= MANE Select	NP_008849.2:p.Val17=
NM_001024956.3:c.50T=	NP_001020127.1:p.Val17=