Canonical Allele Identifier: CA382782619
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs1395596654

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312782T>G , CM000673.2:g.118312782T>G GRCh38
NC_000011.9:g.118183497T>G , CM000673.1:g.118183497T>G GRCh37
NC_000011.8:g.117688707T>G NCBI36
NG_007383.1:g.13203T>G , LRG_38:g.13203T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.268T>G MANE Select ENSP00000354566.4:p.Leu90Val
ENST00000361763.8:c.268T>G ENSP00000354566.4:p.Leu90Val
ENST00000526146.5:n.814T>G
ENST00000528435.5:n.821T>G
ENST00000528600.1:c.250T>G ENSP00000433975.1:p.Leu84Val
ENST00000529713.5:n.374T>G
ENST00000531913.1:n.639T>G
NM_000733.3:c.268T>G , LRG_38t1:c.268T>G NP_000724.1:p.Leu90Val
NM_000733.4:c.268T>G MANE Select NP_000724.1:p.Leu90Val