Canonical Allele Identifier: CA477081957
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183361A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312646A>T , CM000673.2:g.118312646A>T GRCh38
NC_000011.9:g.118183361A>T , CM000673.1:g.118183361A>T GRCh37
NC_000011.8:g.117688571A>T NCBI36
NG_007383.1:g.13067A>T , LRG_38:g.13067A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.132A>T MANE Select ENSP00000354566.4:p.Thr44=
ENST00000361763.8:c.132A>T ENSP00000354566.4:p.Thr44=
ENST00000526146.5:n.678A>T
ENST00000528435.5:n.685A>T
ENST00000528600.1:c.114A>T ENSP00000433975.1:p.Thr38=
ENST00000529713.5:n.238A>T
ENST00000531913.1:n.503A>T
NM_000733.3:c.132A>T , LRG_38t1:c.132A>T NP_000724.1:p.Thr44=
NM_000733.4:c.132A>T MANE Select NP_000724.1:p.Thr44=