Canonical Allele Identifier: CA7650454

Gene: CD276

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73703917G>A , CM000677.2:g.73703917G>A	GRCh38
NC_000015.9:g.73996258G>A , CM000677.1:g.73996258G>A	GRCh37
NC_000015.8:g.71783311G>A	NCBI36
NG_051242.1:g.24952G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001024736.2:c.992G>A MANE Select	NP_001019907.1:p.Arg331His
ENST00000318443.10:c.992G>A MANE Select	ENSP00000320084.5:p.Arg331His
NM_001024736.1:c.992G>A	NP_001019907.1:p.Arg331His
NM_001329628.1:c.419-259G>A	NP_001316557.1:n.419-259G>A
NM_001329628.2:c.419-259G>A	NP_001316557.1:n.419-259G>A
NM_001329629.1:c.554G>A	NP_001316558.1:p.Arg185His
NM_001329629.2:c.554G>A	NP_001316558.1:p.Arg185His
NM_025240.2:c.419-259G>A	NP_079516.1:n.419-259G>A
NM_025240.3:c.419-259G>A	NP_079516.1:n.419-259G>A
ENST00000318424.9:c.419-259G>A	ENSP00000320058.5:n.419-259G>A
ENST00000318443.9:c.992G>A	ENSP00000320084.5:p.Arg331His
ENST00000537340.6:c.554G>A	ENSP00000441087.2:p.Arg185His
ENST00000560928.5:c.*750G>A	ENSP00000453330.1:n.*750G>A
ENST00000561176.5:c.9G>A
ENST00000561213.5:c.992G>A	ENSP00000452736.1:p.Arg331His
ENST00000564751.5:c.419-259G>A	ENSP00000454940.1:n.419-259G>A
XM_005254700.3:c.992G>A	XP_005254757.1:p.Arg331His
XM_005254700.4:c.992G>A	XP_005254757.1:p.Arg331His
XM_011522095.1:c.992G>A	XP_011520397.1:p.Arg331His
XM_011522095.2:c.992G>A	XP_011520397.1:p.Arg331His
XM_011522096.1:c.992G>A	XP_011520398.1:p.Arg331His
XM_017022638.1:c.992G>A	XP_016878127.1:p.Arg331His