Canonical Allele Identifier: CA382781650
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs1422573053

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312618C>A , CM000673.2:g.118312618C>A GRCh38
NC_000011.9:g.118183333C>A , CM000673.1:g.118183333C>A GRCh37
NC_000011.8:g.117688543C>A NCBI36
NG_007383.1:g.13039C>A , LRG_38:g.13039C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361763.9:c.104C>A MANE Select ENSP00000354566.4:p.Pro35Gln
ENST00000361763.8:c.104C>A ENSP00000354566.4:p.Pro35Gln
ENST00000526146.5:n.650C>A
ENST00000528435.5:n.657C>A
ENST00000528600.1:c.86C>A ENSP00000433975.1:p.Ala29Glu
ENST00000529713.5:n.210C>A
ENST00000531913.1:n.475C>A
NM_000733.3:c.104C>A , LRG_38t1:c.104C>A NP_000724.1:p.Pro35Gln
NM_000733.4:c.104C>A MANE Select NP_000724.1:p.Pro35Gln