Canonical Allele Identifier: CA2659958125

Gene: CD8A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86789360_86789362del , CM000664.2:g.86789360_86789362del	GRCh38
NC_000002.11:g.87016483_87016485del , CM000664.1:g.87016483_87016485del	GRCh37
NC_000002.10:g.86869994_86869996del	NCBI36
NG_011608.2:g.24037_24039del , LRG_44:g.24037_24039del

Transcript Alleles

HGVS	Amino-acid Change
NM_001768.7:c.588_590del MANE Select	NP_001759.3:p.Leu197del
ENST00000283635.8:c.588_590del MANE Select	ENSP00000283635.3:p.Leu197del
NM_001145873.1:c.588_590del	NP_001139345.1:p.Leu197del
NM_001382698.1:c.588_590del	NP_001369627.1:p.Leu197del
NM_001768.6:c.588_590del , LRG_44t1:c.588_590del	NP_001759.3:p.Leu197del
NM_171827.3:c.514+280_514+282del	NP_741969.1:n.514+280_514+282del
NM_171827.4:c.514+280_514+282del	NP_741969.1:n.514+280_514+282del
NR_027353.1:n.1063_1065del
NR_027353.2:n.1029_1031del
NR_168478.1:n.2172_2174del
NR_168479.1:n.744-3389_744-3387del
NR_168480.1:n.1944+280_1944+282del
NR_168481.1:n.744-800_744-798del
ENST00000283635.7:c.588_590del	ENSP00000283635.3:p.Leu197del
ENST00000352580.7:c.514+280_514+282del	ENSP00000321631.3:n.514+280_514+282del
ENST00000409511.6:c.588_590del	ENSP00000386559.2:p.Leu197del
ENST00000409781.1:c.477_479del	ENSP00000387314.1:p.Leu160del
ENST00000699436.1:n.1067_1069del
ENST00000699437.1:n.343-800_343-798del
ENST00000699439.1:c.514+280_514+282del	ENSP00000514390.1:n.514+280_514+282del