Canonical Allele Identifier: CA382782595
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183490T>A (hg19) chr11:g.118312775T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312775T>A , CM000673.2:g.118312775T>A GRCh38
NC_000011.9:g.118183490T>A , CM000673.1:g.118183490T>A GRCh37
NC_000011.8:g.117688700T>A NCBI36
NG_007383.1:g.13196T>A , LRG_38:g.13196T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.261T>A MANE Select ENSP00000354566.4:p.Phe87Leu
ENST00000361763.8:c.261T>A ENSP00000354566.4:p.Phe87Leu
ENST00000526146.5:n.807T>A
ENST00000528435.5:n.814T>A
ENST00000528600.1:c.243T>A ENSP00000433975.1:p.Phe81Leu
ENST00000529713.5:n.367T>A
ENST00000531913.1:n.632T>A
NM_000733.3:c.261T>A , LRG_38t1:c.261T>A NP_000724.1:p.Phe87Leu
NM_000733.4:c.261T>A MANE Select NP_000724.1:p.Phe87Leu
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