Canonical Allele Identifier: CA382781705
Gene: CD3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312629T>A , CM000673.2:g.118312629T>A GRCh38
NC_000011.9:g.118183344T>A , CM000673.1:g.118183344T>A GRCh37
NC_000011.8:g.117688554T>A NCBI36
NG_007383.1:g.13050T>A , LRG_38:g.13050T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.115T>A MANE Select ENSP00000354566.4:p.Ser39Thr
ENST00000361763.8:c.115T>A ENSP00000354566.4:p.Ser39Thr
ENST00000526146.5:n.661T>A
ENST00000528435.5:n.668T>A
ENST00000528600.1:c.97T>A ENSP00000433975.1:p.Ser33Thr
ENST00000529713.5:n.221T>A
ENST00000531913.1:n.486T>A
NM_000733.3:c.115T>A , LRG_38t1:c.115T>A NP_000724.1:p.Ser39Thr
NM_000733.4:c.115T>A MANE Select NP_000724.1:p.Ser39Thr