Canonical Allele Identifier: CA427168639

Gene: CD8A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86790787G>A , CM000664.2:g.86790787G>A	GRCh38
NC_000002.11:g.87017910G>A , CM000664.1:g.87017910G>A	GRCh37
NC_000002.10:g.86871421G>A	NCBI36
NG_011608.2:g.22610C>T , LRG_44:g.22610C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001768.7:c.39C>T MANE Select	NP_001759.3:p.Ala13=
ENST00000283635.8:c.39C>T MANE Select	ENSP00000283635.3:p.Ala13=
NM_001145873.1:c.39C>T	NP_001139345.1:p.Ala13=
NM_001382698.1:c.39C>T	NP_001369627.1:p.Ala13=
NM_001768.6:c.39C>T , LRG_44t1:c.39C>T	NP_001759.3:p.Ala13=
NM_171827.3:c.39C>T	NP_741969.1:p.Ala13=
NM_171827.4:c.39C>T	NP_741969.1:p.Ala13=
NR_027353.1:n.514C>T
NR_027353.2:n.480C>T
NR_168478.1:n.1623C>T
NR_168479.1:n.744-4816C>T
NR_168480.1:n.1469C>T
NR_168481.1:n.744-2227C>T
ENST00000283635.7:c.39C>T	ENSP00000283635.3:p.Ala13=
ENST00000352580.7:c.39C>T	ENSP00000321631.3:p.Ala13=
ENST00000409511.6:c.39C>T	ENSP00000386559.2:p.Ala13=
ENST00000409781.1:c.39C>T	ENSP00000387314.1:p.Ala13=
ENST00000699436.1:n.518C>T
ENST00000699437.1:n.343-2227C>T
ENST00000699439.1:c.39C>T	ENSP00000514390.1:p.Ala13=