Canonical Allele Identifier: CA393099535

Gene: CD276

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73704286T>C , CM000677.2:g.73704286T>C	GRCh38
NC_000015.9:g.73996627T>C , CM000677.1:g.73996627T>C	GRCh37
NC_000015.8:g.71783680T>C	NCBI36
NG_051242.1:g.25321T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001024736.2:c.1183T>C MANE Select	NP_001019907.1:p.Phe395Leu
ENST00000318443.10:c.1183T>C MANE Select	ENSP00000320084.5:p.Phe395Leu
NM_001024736.1:c.1183T>C	NP_001019907.1:p.Phe395Leu
NM_001329628.1:c.529T>C	NP_001316557.1:p.Phe177Leu
NM_001329628.2:c.529T>C	NP_001316557.1:p.Phe177Leu
NM_001329629.1:c.745T>C	NP_001316558.1:p.Phe249Leu
NM_001329629.2:c.745T>C	NP_001316558.1:p.Phe249Leu
NM_025240.2:c.529T>C	NP_079516.1:p.Phe177Leu
NM_025240.3:c.529T>C	NP_079516.1:p.Phe177Leu
ENST00000318424.9:c.529T>C	ENSP00000320058.5:p.Phe177Leu
ENST00000318443.9:c.1183T>C	ENSP00000320084.5:p.Phe395Leu
ENST00000537340.6:c.745T>C	ENSP00000441087.2:p.Phe249Leu
ENST00000557951.1:n.158T>C
ENST00000559073.1:c.90T>C
ENST00000560928.5:c.*941T>C	ENSP00000453330.1:n.*941T>C
ENST00000561176.5:c.200T>C
ENST00000561213.5:c.1183T>C	ENSP00000452736.1:p.Phe395Leu
ENST00000564751.5:c.529T>C	ENSP00000454940.1:p.Phe177Leu
XM_005254700.3:c.1183T>C	XP_005254757.1:p.Phe395Leu
XM_005254700.4:c.1183T>C	XP_005254757.1:p.Phe395Leu
XM_011522095.1:c.1183T>C	XP_011520397.1:p.Phe395Leu
XM_011522095.2:c.1183T>C	XP_011520397.1:p.Phe395Leu
XM_011522096.1:c.1183T>C	XP_011520398.1:p.Phe395Leu
XM_017022638.1:c.1183T>C	XP_016878127.1:p.Phe395Leu