Canonical Allele Identifier: CA427165987

Gene: CD8A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86789357_86789359del , CM000664.2:g.86789357_86789359del	GRCh38
NC_000002.11:g.87016480_87016482del , CM000664.1:g.87016480_87016482del	GRCh37
NC_000002.10:g.86869991_86869993del	NCBI36
NG_011608.2:g.24040_24042del , LRG_44:g.24040_24042del

Transcript Alleles

HGVS	Amino-acid Change
NM_001768.7:c.591_593del MANE Select	NP_001759.3:p.Leu198del
ENST00000283635.8:c.591_593del MANE Select	ENSP00000283635.3:p.Leu198del
NM_001145873.1:c.591_593del	NP_001139345.1:p.Leu198del
NM_001382698.1:c.591_593del	NP_001369627.1:p.Leu198del
NM_001768.6:c.591_593del , LRG_44t1:c.591_593del	NP_001759.3:p.Leu198del
NM_171827.3:c.514+283_514+285del	NP_741969.1:n.514+283_514+285del
NM_171827.4:c.514+283_514+285del	NP_741969.1:n.514+283_514+285del
NR_027353.1:n.1066_1068del
NR_027353.2:n.1032_1034del
NR_168478.1:n.2175_2177del
NR_168479.1:n.744-3386_744-3384del
NR_168480.1:n.1944+283_1944+285del
NR_168481.1:n.744-797_744-795del
ENST00000283635.7:c.591_593del	ENSP00000283635.3:p.Leu198del
ENST00000352580.7:c.514+283_514+285del	ENSP00000321631.3:n.514+283_514+285del
ENST00000409511.6:c.591_593del	ENSP00000386559.2:p.Leu198del
ENST00000409781.1:c.480_482del	ENSP00000387314.1:p.Leu161del
ENST00000699436.1:n.1070_1072del
ENST00000699437.1:n.343-797_343-795del
ENST00000699439.1:c.514+283_514+285del	ENSP00000514390.1:n.514+283_514+285del