Canonical Allele Identifier: CA393099064

Gene: CD276

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73703977C>T , CM000677.2:g.73703977C>T	GRCh38
NC_000015.9:g.73996318C>T , CM000677.1:g.73996318C>T	GRCh37
NC_000015.8:g.71783371C>T	NCBI36
NG_051242.1:g.25012C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001024736.2:c.1052C>T MANE Select	NP_001019907.1:p.Ala351Val
ENST00000318443.10:c.1052C>T MANE Select	ENSP00000320084.5:p.Ala351Val
NM_001024736.1:c.1052C>T	NP_001019907.1:p.Ala351Val
NM_001329628.1:c.419-199C>T	NP_001316557.1:n.419-199C>T
NM_001329628.2:c.419-199C>T	NP_001316557.1:n.419-199C>T
NM_001329629.1:c.614C>T	NP_001316558.1:p.Ala205Val
NM_001329629.2:c.614C>T	NP_001316558.1:p.Ala205Val
NM_025240.2:c.419-199C>T	NP_079516.1:n.419-199C>T
NM_025240.3:c.419-199C>T	NP_079516.1:n.419-199C>T
ENST00000318424.9:c.419-199C>T	ENSP00000320058.5:n.419-199C>T
ENST00000318443.9:c.1052C>T	ENSP00000320084.5:p.Ala351Val
ENST00000537340.6:c.614C>T	ENSP00000441087.2:p.Ala205Val
ENST00000557951.1:n.27C>T
ENST00000560928.5:c.*810C>T	ENSP00000453330.1:n.*810C>T
ENST00000561176.5:c.69C>T
ENST00000561213.5:c.1052C>T	ENSP00000452736.1:p.Ala351Val
ENST00000564751.5:c.419-199C>T	ENSP00000454940.1:n.419-199C>T
XM_005254700.3:c.1052C>T	XP_005254757.1:p.Ala351Val
XM_005254700.4:c.1052C>T	XP_005254757.1:p.Ala351Val
XM_011522095.1:c.1052C>T	XP_011520397.1:p.Ala351Val
XM_011522095.2:c.1052C>T	XP_011520397.1:p.Ala351Val
XM_011522096.1:c.1052C>T	XP_011520398.1:p.Ala351Val
XM_017022638.1:c.1052C>T	XP_016878127.1:p.Ala351Val