Canonical Allele Identifier: CA2187339665

Gene: CD276

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73685996C>G , CM000677.2:g.73685996C>G	GRCh38
NC_000015.9:g.73978337C>G , CM000677.1:g.73978337C>G	GRCh37
NC_000015.8:g.71765390C>G	NCBI36
NG_051242.1:g.7031C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318443.10:c.-55+1536C>G MANE Select	ENSP00000320084.5:n.-55+1536C>G
ENST00000318424.9:c.-55+1536C>G	ENSP00000320058.5:n.-55+1536C>G
ENST00000318443.9:c.-55+1536C>G	ENSP00000320084.5:n.-55+1536C>G
ENST00000537340.6:c.-360+1536C>G	ENSP00000441087.2:n.-360+1536C>G
ENST00000558689.5:c.-162+1536C>G	ENSP00000453907.1:n.-162+1536C>G
ENST00000560786.6:c.-55+1589C>G	ENSP00000452649.2:n.-55+1589C>G
ENST00000560928.5:c.-55+1536C>G	ENSP00000453330.1:n.-55+1536C>G
ENST00000560995.5:c.-55+1097C>G	ENSP00000453336.1:n.-55+1097C>G
ENST00000561213.5:c.-55+1536C>G	ENSP00000452736.1:n.-55+1536C>G
ENST00000561260.5:c.-55+913C>G	ENSP00000452669.1:n.-55+913C>G
ENST00000561416.5:c.-55+1197C>G	ENSP00000452905.1:n.-55+1197C>G
ENST00000563584.5:c.-44+1536C>G	ENSP00000454258.1:n.-44+1536C>G
ENST00000567189.5:c.-55+1933C>G	ENSP00000455366.1:n.-55+1933C>G
ENST00000567582.5:c.-55+1197C>G	ENSP00000456657.1:n.-55+1197C>G
NM_001024736.1:c.-55+1536C>G	NP_001019907.1:n.-55+1536C>G
NM_025240.2:c.-55+1536C>G	NP_079516.1:n.-55+1536C>G
XM_005254700.3:c.-55+1197C>G	XP_005254757.1:n.-55+1197C>G
XM_011522095.1:c.-55+1097C>G	XP_011520397.1:n.-55+1097C>G
NM_001329628.1:c.-55+1097C>G	NP_001316557.1:n.-55+1097C>G
NM_001329629.1:c.-360+1536C>G	NP_001316558.1:n.-360+1536C>G
XM_005254700.4:c.-55+1197C>G	XP_005254757.1:n.-55+1197C>G
XM_011522095.2:c.-55+1097C>G	XP_011520397.1:n.-55+1097C>G
XM_017022638.1:c.-55+1933C>G	XP_016878127.1:n.-55+1933C>G
NM_001024736.2:c.-55+1536C>G MANE Select	NP_001019907.1:n.-55+1536C>G
NM_001329628.2:c.-55+1097C>G	NP_001316557.1:n.-55+1097C>G
NM_001329629.2:c.-360+1536C>G	NP_001316558.1:n.-360+1536C>G
NM_025240.3:c.-55+1536C>G	NP_079516.1:n.-55+1536C>G