Canonical Allele Identifier: CA7650578

Gene: CD276

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73704431C>G , CM000677.2:g.73704431C>G	GRCh38
NC_000015.9:g.73996772C>G , CM000677.1:g.73996772C>G	GRCh37
NC_000015.8:g.71783825C>G	NCBI36
NG_051242.1:g.25466C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001024736.2:c.1328C>G MANE Select	NP_001019907.1:p.Pro443Arg
ENST00000318443.10:c.1328C>G MANE Select	ENSP00000320084.5:p.Pro443Arg
NM_001024736.1:c.1328C>G	NP_001019907.1:p.Pro443Arg
NM_001329628.1:c.674C>G	NP_001316557.1:p.Pro225Arg
NM_001329628.2:c.674C>G	NP_001316557.1:p.Pro225Arg
NM_001329629.1:c.890C>G	NP_001316558.1:p.Pro297Arg
NM_001329629.2:c.890C>G	NP_001316558.1:p.Pro297Arg
NM_025240.2:c.674C>G	NP_079516.1:p.Pro225Arg
NM_025240.3:c.674C>G	NP_079516.1:p.Pro225Arg
ENST00000318424.9:c.674C>G	ENSP00000320058.5:p.Pro225Arg
ENST00000318443.9:c.1328C>G	ENSP00000320084.5:p.Pro443Arg
ENST00000537340.6:c.890C>G	ENSP00000441087.2:p.Pro297Arg
ENST00000557951.1:n.303C>G
ENST00000559073.1:c.235C>G
ENST00000560928.5:c.*1086C>G	ENSP00000453330.1:n.*1086C>G
ENST00000561176.5:c.345C>G
ENST00000561213.5:c.1328C>G	ENSP00000452736.1:p.Pro443Arg
ENST00000564751.5:c.674C>G	ENSP00000454940.1:p.Pro225Arg
XM_005254700.3:c.1328C>G	XP_005254757.1:p.Pro443Arg
XM_005254700.4:c.1328C>G	XP_005254757.1:p.Pro443Arg
XM_011522095.1:c.1328C>G	XP_011520397.1:p.Pro443Arg
XM_011522095.2:c.1328C>G	XP_011520397.1:p.Pro443Arg
XM_011522096.1:c.1328C>G	XP_011520398.1:p.Pro443Arg
XM_017022638.1:c.1328C>G	XP_016878127.1:p.Pro443Arg