Canonical Allele Identifier: CA477081940
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183346C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312631C>A , CM000673.2:g.118312631C>A GRCh38
NC_000011.9:g.118183346C>A , CM000673.1:g.118183346C>A GRCh37
NC_000011.8:g.117688556C>A NCBI36
NG_007383.1:g.13052C>A , LRG_38:g.13052C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.117C>A MANE Select ENSP00000354566.4:p.Ser39=
ENST00000361763.8:c.117C>A ENSP00000354566.4:p.Ser39=
ENST00000526146.5:n.663C>A
ENST00000528435.5:n.670C>A
ENST00000528600.1:c.99C>A ENSP00000433975.1:p.Ser33=
ENST00000529713.5:n.223C>A
ENST00000531913.1:n.488C>A
NM_000733.3:c.117C>A , LRG_38t1:c.117C>A NP_000724.1:p.Ser39=
NM_000733.4:c.117C>A MANE Select NP_000724.1:p.Ser39=