Canonical Allele Identifier: CA382781658
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs1397810052

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312620T>A , CM000673.2:g.118312620T>A GRCh38
NC_000011.9:g.118183335T>A , CM000673.1:g.118183335T>A GRCh37
NC_000011.8:g.117688545T>A NCBI36
NG_007383.1:g.13041T>A , LRG_38:g.13041T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361763.9:c.106T>A MANE Select ENSP00000354566.4:p.Tyr36Asn
ENST00000361763.8:c.106T>A ENSP00000354566.4:p.Tyr36Asn
ENST00000526146.5:n.652T>A
ENST00000528435.5:n.659T>A
ENST00000528600.1:c.88T>A ENSP00000433975.1:p.Tyr30Asn
ENST00000529713.5:n.212T>A
ENST00000531913.1:n.477T>A
NM_000733.3:c.106T>A , LRG_38t1:c.106T>A NP_000724.1:p.Tyr36Asn
NM_000733.4:c.106T>A MANE Select NP_000724.1:p.Tyr36Asn