Canonical Allele Identifier: CA393095740

Gene: CD276

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73702341C>T , CM000677.2:g.73702341C>T	GRCh38
NC_000015.9:g.73994682C>T , CM000677.1:g.73994682C>T	GRCh37
NC_000015.8:g.71781735C>T	NCBI36
NG_051242.1:g.23376C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001024736.2:c.166C>T MANE Select	NP_001019907.1:p.Pro56Ser
ENST00000318443.10:c.166C>T MANE Select	ENSP00000320084.5:p.Pro56Ser
NM_001024736.1:c.166C>T	NP_001019907.1:p.Pro56Ser
NM_001329628.1:c.166C>T	NP_001316557.1:p.Pro56Ser
NM_001329628.2:c.166C>T	NP_001316557.1:p.Pro56Ser
NM_001329629.1:c.-273C>T	NP_001316558.1:n.-273C>T
NM_001329629.2:c.-273C>T	NP_001316558.1:n.-273C>T
NM_025240.2:c.166C>T	NP_079516.1:p.Pro56Ser
NM_025240.3:c.166C>T	NP_079516.1:p.Pro56Ser
ENST00000318424.9:c.166C>T	ENSP00000320058.5:p.Pro56Ser
ENST00000318443.9:c.166C>T	ENSP00000320084.5:p.Pro56Ser
ENST00000537340.6:c.-273C>T	ENSP00000441087.2:n.-273C>T
ENST00000558689.5:c.166C>T	ENSP00000453907.1:p.Pro56Ser
ENST00000560786.6:c.166C>T	ENSP00000452649.2:p.Pro56Ser
ENST00000560928.5:c.80-39C>T	ENSP00000453330.1:n.80-39C>T
ENST00000560995.5:c.166C>T	ENSP00000453336.1:p.Pro56Ser
ENST00000561213.5:c.166C>T	ENSP00000452736.1:p.Pro56Ser
ENST00000561260.5:c.166C>T	ENSP00000452669.1:p.Pro56Ser
ENST00000563584.5:c.283C>T	ENSP00000454258.1:p.Pro95Ser
ENST00000564751.5:c.166C>T	ENSP00000454940.1:p.Pro56Ser
ENST00000567189.5:c.166C>T	ENSP00000455366.1:p.Pro56Ser
ENST00000567582.5:c.80-39C>T	ENSP00000456657.1:n.80-39C>T
XM_005254700.3:c.166C>T	XP_005254757.1:p.Pro56Ser
XM_005254700.4:c.166C>T	XP_005254757.1:p.Pro56Ser
XM_011522095.1:c.166C>T	XP_011520397.1:p.Pro56Ser
XM_011522095.2:c.166C>T	XP_011520397.1:p.Pro56Ser
XM_011522096.1:c.166C>T	XP_011520398.1:p.Pro56Ser
XM_017022638.1:c.166C>T	XP_016878127.1:p.Pro56Ser