Canonical Allele Identifier: CA382781985
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183401C>A (hg19) chr11:g.118312686C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312686C>A , CM000673.2:g.118312686C>A GRCh38
NC_000011.9:g.118183401C>A , CM000673.1:g.118183401C>A GRCh37
NC_000011.8:g.117688611C>A NCBI36
NG_007383.1:g.13107C>A , LRG_38:g.13107C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.172C>A MANE Select ENSP00000354566.4:p.Leu58Ile
ENST00000361763.8:c.172C>A ENSP00000354566.4:p.Leu58Ile
ENST00000526146.5:n.718C>A
ENST00000528435.5:n.725C>A
ENST00000528600.1:c.154C>A ENSP00000433975.1:p.Leu52Ile
ENST00000529713.5:n.278C>A
ENST00000531913.1:n.543C>A
NM_000733.3:c.172C>A , LRG_38t1:c.172C>A NP_000724.1:p.Leu58Ile
NM_000733.4:c.172C>A MANE Select NP_000724.1:p.Leu58Ile
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