Canonical Allele Identifier: CA150567
Gene: CD3E HGNC NCBI

Linked Data

ClinVar Variation Id: 12745
ClinVar RCV Id: RCV000087025
dbSNP Id: rs121918659

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312690G>A , CM000673.2:g.118312690G>A GRCh38
NC_000011.9:g.118183405G>A , CM000673.1:g.118183405G>A GRCh37
NC_000011.8:g.117688615G>A NCBI36
NG_007383.1:g.13111G>A , LRG_38:g.13111G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361763.9:c.176G>A MANE Select ENSP00000354566.4:p.Trp59Ter
ENST00000361763.8:c.176G>A ENSP00000354566.4:p.Trp59Ter
ENST00000526146.5:n.722G>A
ENST00000528435.5:n.729G>A
ENST00000528600.1:c.158G>A ENSP00000433975.1:p.Trp53Ter
ENST00000529713.5:n.282G>A
ENST00000531913.1:n.547G>A
NM_000733.3:c.176G>A , LRG_38t1:c.176G>A NP_000724.1:p.Trp59Ter
NM_000733.4:c.176G>A MANE Select NP_000724.1:p.Trp59Ter