Canonical Allele Identifier: CA477081984
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183394T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312679T>A , CM000673.2:g.118312679T>A GRCh38
NC_000011.9:g.118183394T>A , CM000673.1:g.118183394T>A GRCh37
NC_000011.8:g.117688604T>A NCBI36
NG_007383.1:g.13100T>A , LRG_38:g.13100T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.165T>A MANE Select ENSP00000354566.4:p.Ser55=
ENST00000361763.8:c.165T>A ENSP00000354566.4:p.Ser55=
ENST00000526146.5:n.711T>A
ENST00000528435.5:n.718T>A
ENST00000528600.1:c.147T>A ENSP00000433975.1:p.Ser49=
ENST00000529713.5:n.271T>A
ENST00000531913.1:n.536T>A
NM_000733.3:c.165T>A , LRG_38t1:c.165T>A NP_000724.1:p.Ser55=
NM_000733.4:c.165T>A MANE Select NP_000724.1:p.Ser55=
Search 100 bp 5'
Search 100 bp 3'