Canonical Allele Identifier: CA6301628
Gene: CD3E HGNC NCBI

Linked Data

ClinVar Variation Id: 1465746
dbSNP Id: rs369130631

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312630C>A , CM000673.2:g.118312630C>A GRCh38
NC_000011.9:g.118183345C>A , CM000673.1:g.118183345C>A GRCh37
NC_000011.8:g.117688555C>A NCBI36
NG_007383.1:g.13051C>A , LRG_38:g.13051C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.116C>A MANE Select ENSP00000354566.4:p.Ser39Tyr
ENST00000361763.8:c.116C>A ENSP00000354566.4:p.Ser39Tyr
ENST00000526146.5:n.662C>A
ENST00000528435.5:n.669C>A
ENST00000528600.1:c.98C>A ENSP00000433975.1:p.Ser33Tyr
ENST00000529713.5:n.222C>A
ENST00000531913.1:n.487C>A
NM_000733.3:c.116C>A , LRG_38t1:c.116C>A NP_000724.1:p.Ser39Tyr
NM_000733.4:c.116C>A MANE Select NP_000724.1:p.Ser39Tyr