Canonical Allele Identifier: CA477081965
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183370G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312655G>A , CM000673.2:g.118312655G>A GRCh38
NC_000011.9:g.118183370G>A , CM000673.1:g.118183370G>A GRCh37
NC_000011.8:g.117688580G>A NCBI36
NG_007383.1:g.13076G>A , LRG_38:g.13076G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.141G>A MANE Select ENSP00000354566.4:p.Leu47=
ENST00000361763.8:c.141G>A ENSP00000354566.4:p.Leu47=
ENST00000526146.5:n.687G>A
ENST00000528435.5:n.694G>A
ENST00000528600.1:c.123G>A ENSP00000433975.1:p.Leu41=
ENST00000529713.5:n.247G>A
ENST00000531913.1:n.512G>A
NM_000733.3:c.141G>A , LRG_38t1:c.141G>A NP_000724.1:p.Leu47=
NM_000733.4:c.141G>A MANE Select NP_000724.1:p.Leu47=
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