Canonical Allele Identifier: CA382782585
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs1357486248

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312774T>A , CM000673.2:g.118312774T>A GRCh38
NC_000011.9:g.118183489T>A , CM000673.1:g.118183489T>A GRCh37
NC_000011.8:g.117688699T>A NCBI36
NG_007383.1:g.13195T>A , LRG_38:g.13195T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.260T>A MANE Select ENSP00000354566.4:p.Phe87Tyr
ENST00000361763.8:c.260T>A ENSP00000354566.4:p.Phe87Tyr
ENST00000526146.5:n.806T>A
ENST00000528435.5:n.813T>A
ENST00000528600.1:c.242T>A ENSP00000433975.1:p.Phe81Tyr
ENST00000529713.5:n.366T>A
ENST00000531913.1:n.631T>A
NM_000733.3:c.260T>A , LRG_38t1:c.260T>A NP_000724.1:p.Phe87Tyr
NM_000733.4:c.260T>A MANE Select NP_000724.1:p.Phe87Tyr