Canonical Allele Identifier: CA393096156

Gene: CD276

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73702541C>G , CM000677.2:g.73702541C>G	GRCh38
NC_000015.9:g.73994882C>G , CM000677.1:g.73994882C>G	GRCh37
NC_000015.8:g.71781935C>G	NCBI36
NG_051242.1:g.23576C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001024736.2:c.366C>G MANE Select	NP_001019907.1:p.Cys122Trp
ENST00000318443.10:c.366C>G MANE Select	ENSP00000320084.5:p.Cys122Trp
NM_001024736.1:c.366C>G	NP_001019907.1:p.Cys122Trp
NM_001329628.1:c.366C>G	NP_001316557.1:p.Cys122Trp
NM_001329628.2:c.366C>G	NP_001316557.1:p.Cys122Trp
NM_001329629.1:c.-73C>G	NP_001316558.1:n.-73C>G
NM_001329629.2:c.-73C>G	NP_001316558.1:n.-73C>G
NM_025240.2:c.366C>G	NP_079516.1:p.Cys122Trp
NM_025240.3:c.366C>G	NP_079516.1:p.Cys122Trp
ENST00000318424.9:c.366C>G	ENSP00000320058.5:p.Cys122Trp
ENST00000318443.9:c.366C>G	ENSP00000320084.5:p.Cys122Trp
ENST00000537340.6:c.-73C>G	ENSP00000441087.2:n.-73C>G
ENST00000558689.5:c.366C>G	ENSP00000453907.1:p.Cys122Trp
ENST00000560786.6:c.366C>G	ENSP00000452649.2:p.Cys122Trp
ENST00000560928.5:c.*124C>G	ENSP00000453330.1:n.*124C>G
ENST00000560995.5:c.366C>G	ENSP00000453336.1:p.Cys122Trp
ENST00000561213.5:c.366C>G	ENSP00000452736.1:p.Cys122Trp
ENST00000561260.5:c.366C>G	ENSP00000452669.1:p.Cys122Trp
ENST00000564751.5:c.366C>G	ENSP00000454940.1:p.Cys122Trp
ENST00000567189.5:c.366C>G	ENSP00000455366.1:p.Cys122Trp
ENST00000567582.5:c.*124C>G	ENSP00000456657.1:n.*124C>G
XM_005254700.3:c.366C>G	XP_005254757.1:p.Cys122Trp
XM_005254700.4:c.366C>G	XP_005254757.1:p.Cys122Trp
XM_011522095.1:c.366C>G	XP_011520397.1:p.Cys122Trp
XM_011522095.2:c.366C>G	XP_011520397.1:p.Cys122Trp
XM_011522096.1:c.366C>G	XP_011520398.1:p.Cys122Trp
XM_017022638.1:c.366C>G	XP_016878127.1:p.Cys122Trp