Canonical Allele Identifier: CA2004808856

Gene: SC5D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121303400G= , CM000673.2:g.121303400G=	GRCh38
NC_000011.9:g.121174109G= , CM000673.1:g.121174109G=	GRCh37
NC_000011.8:g.120679319G=	NCBI36
NG_009446.1:g.15722G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.25G= MANE Select	ENSP00000264027.4:p.Asp9=
ENST00000264027.8:c.25G=	ENSP00000264027.4:p.Asp9=
ENST00000392789.2:c.25G=	ENSP00000376539.2:p.Asp9=
ENST00000524683.5:n.81G=
ENST00000527762.5:c.25G=	ENSP00000436290.1:p.Asp9=
ENST00000531140.1:n.93G=
ENST00000534230.5:c.25G=	ENSP00000432550.1:p.Asp9=
ENST00000534455.5:n.171G=
NM_001024956.2:c.25G=	NP_001020127.1:p.Asp9=
NM_006918.4:c.25G=	NP_008849.2:p.Asp9=
NM_006918.5:c.25G= MANE Select	NP_008849.2:p.Asp9=
NM_001024956.3:c.25G=	NP_001020127.1:p.Asp9=