Canonical Allele Identifier: CA7650617

Gene: CD276

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73708374G>A , CM000677.2:g.73708374G>A	GRCh38
NC_000015.9:g.74000715G>A , CM000677.1:g.74000715G>A	GRCh37
NC_000015.8:g.71787768G>A	NCBI36
NG_051242.1:g.29409G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001024736.2:c.1405G>A MANE Select	NP_001019907.1:p.Val469Met
ENST00000318443.10:c.1405G>A MANE Select	ENSP00000320084.5:p.Val469Met
NM_001024736.1:c.1405G>A	NP_001019907.1:p.Val469Met
NM_001329628.1:c.751G>A	NP_001316557.1:p.Val251Met
NM_001329628.2:c.751G>A	NP_001316557.1:p.Val251Met
NM_001329629.1:c.967G>A	NP_001316558.1:p.Val323Met
NM_001329629.2:c.967G>A	NP_001316558.1:p.Val323Met
NM_025240.2:c.751G>A	NP_079516.1:p.Val251Met
NM_025240.3:c.751G>A	NP_079516.1:p.Val251Met
ENST00000318424.9:c.751G>A	ENSP00000320058.5:p.Val251Met
ENST00000318443.9:c.1405G>A	ENSP00000320084.5:p.Val469Met
ENST00000537340.6:c.967G>A	ENSP00000441087.2:p.Val323Met
ENST00000557951.1:n.380G>A
ENST00000559073.1:c.312G>A
ENST00000560928.5:c.*1163G>A	ENSP00000453330.1:n.*1163G>A
ENST00000561176.5:c.398G>A
ENST00000561213.5:c.1405G>A	ENSP00000452736.1:p.Val469Met
ENST00000564751.5:c.751G>A	ENSP00000454940.1:p.Val251Met
XM_005254700.3:c.1405G>A	XP_005254757.1:p.Val469Met
XM_005254700.4:c.1405G>A	XP_005254757.1:p.Val469Met
XM_011522095.1:c.1405G>A	XP_011520397.1:p.Val469Met
XM_011522095.2:c.1405G>A	XP_011520397.1:p.Val469Met
XM_011522096.1:c.1405G>A	XP_011520398.1:p.Val469Met
XM_017022638.1:c.1405G>A	XP_016878127.1:p.Val469Met