Canonical Allele Identifier: CA894077388

Gene: CD8A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86789759G>A , CM000664.2:g.86789759G>A	GRCh38
NC_000002.11:g.87016882G>A , CM000664.1:g.87016882G>A	GRCh37
NC_000002.10:g.86870393G>A	NCBI36
NG_011608.2:g.23638C>T , LRG_44:g.23638C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001768.7:c.404-9C>T MANE Select	NP_001759.3:n.404-9C>T
ENST00000283635.8:c.404-9C>T MANE Select	ENSP00000283635.3:n.404-9C>T
NM_001145873.1:c.404-9C>T	NP_001139345.1:n.404-9C>T
NM_001382698.1:c.404-9C>T	NP_001369627.1:n.404-9C>T
NM_001768.6:c.404-9C>T , LRG_44t1:c.404-9C>T	NP_001759.3:n.404-9C>T
NM_171827.3:c.404-9C>T	NP_741969.1:n.404-9C>T
NM_171827.4:c.404-9C>T	NP_741969.1:n.404-9C>T
NR_027353.1:n.879-9C>T
NR_027353.2:n.845-9C>T
NR_168478.1:n.1988-9C>T
NR_168479.1:n.744-3788C>T
NR_168480.1:n.1834-9C>T
NR_168481.1:n.744-1199C>T
ENST00000283635.7:c.404-9C>T	ENSP00000283635.3:n.404-9C>T
ENST00000352580.7:c.404-9C>T	ENSP00000321631.3:n.404-9C>T
ENST00000409511.6:c.404-9C>T	ENSP00000386559.2:n.404-9C>T
ENST00000409781.1:c.404-326C>T	ENSP00000387314.1:n.404-326C>T
ENST00000699436.1:n.883-9C>T
ENST00000699437.1:n.343-1199C>T
ENST00000699439.1:c.404-9C>T	ENSP00000514390.1:n.404-9C>T