Canonical Allele Identifier: CA7650512

Gene: CD276

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73704224G>A , CM000677.2:g.73704224G>A	GRCh38
NC_000015.9:g.73996565G>A , CM000677.1:g.73996565G>A	GRCh37
NC_000015.8:g.71783618G>A	NCBI36
NG_051242.1:g.25259G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001024736.2:c.1121G>A MANE Select	NP_001019907.1:p.Arg374Gln
ENST00000318443.10:c.1121G>A MANE Select	ENSP00000320084.5:p.Arg374Gln
NM_001024736.1:c.1121G>A	NP_001019907.1:p.Arg374Gln
NM_001329628.1:c.467G>A	NP_001316557.1:p.Arg156Gln
NM_001329628.2:c.467G>A	NP_001316557.1:p.Arg156Gln
NM_001329629.1:c.683G>A	NP_001316558.1:p.Arg228Gln
NM_001329629.2:c.683G>A	NP_001316558.1:p.Arg228Gln
NM_025240.2:c.467G>A	NP_079516.1:p.Arg156Gln
NM_025240.3:c.467G>A	NP_079516.1:p.Arg156Gln
ENST00000318424.9:c.467G>A	ENSP00000320058.5:p.Arg156Gln
ENST00000318443.9:c.1121G>A	ENSP00000320084.5:p.Arg374Gln
ENST00000537340.6:c.683G>A	ENSP00000441087.2:p.Arg228Gln
ENST00000557951.1:n.96G>A
ENST00000559073.1:c.28G>A
ENST00000560928.5:c.*879G>A	ENSP00000453330.1:n.*879G>A
ENST00000561176.5:c.138G>A
ENST00000561213.5:c.1121G>A	ENSP00000452736.1:p.Arg374Gln
ENST00000564751.5:c.467G>A	ENSP00000454940.1:p.Arg156Gln
XM_005254700.3:c.1121G>A	XP_005254757.1:p.Arg374Gln
XM_005254700.4:c.1121G>A	XP_005254757.1:p.Arg374Gln
XM_011522095.1:c.1121G>A	XP_011520397.1:p.Arg374Gln
XM_011522095.2:c.1121G>A	XP_011520397.1:p.Arg374Gln
XM_011522096.1:c.1121G>A	XP_011520398.1:p.Arg374Gln
XM_017022638.1:c.1121G>A	XP_016878127.1:p.Arg374Gln