Canonical Allele Identifier: CA427166653

Gene: CD8A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86789710C>T , CM000664.2:g.86789710C>T	GRCh38
NC_000002.11:g.87016833C>T , CM000664.1:g.87016833C>T	GRCh37
NC_000002.10:g.86870344C>T	NCBI36
NG_011608.2:g.23687G>A , LRG_44:g.23687G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001768.7:c.444G>A MANE Select	NP_001759.3:p.Pro148=
ENST00000283635.8:c.444G>A MANE Select	ENSP00000283635.3:p.Pro148=
NM_001145873.1:c.444G>A	NP_001139345.1:p.Pro148=
NM_001382698.1:c.444G>A	NP_001369627.1:p.Pro148=
NM_001768.6:c.444G>A , LRG_44t1:c.444G>A	NP_001759.3:p.Pro148=
NM_171827.3:c.444G>A	NP_741969.1:p.Pro148=
NM_171827.4:c.444G>A	NP_741969.1:p.Pro148=
NR_027353.1:n.919G>A
NR_027353.2:n.885G>A
NR_168478.1:n.2028G>A
NR_168479.1:n.744-3739G>A
NR_168480.1:n.1874G>A
NR_168481.1:n.744-1150G>A
ENST00000283635.7:c.444G>A	ENSP00000283635.3:p.Pro148=
ENST00000352580.7:c.444G>A	ENSP00000321631.3:p.Pro148=
ENST00000409511.6:c.444G>A	ENSP00000386559.2:p.Pro148=
ENST00000409781.1:c.404-277G>A	ENSP00000387314.1:n.404-277G>A
ENST00000699436.1:n.923G>A
ENST00000699437.1:n.343-1150G>A
ENST00000699439.1:c.444G>A	ENSP00000514390.1:p.Pro148=