Canonical Allele Identifier: CA382782592
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183489T>G (hg19) chr11:g.118312774T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312774T>G , CM000673.2:g.118312774T>G GRCh38
NC_000011.9:g.118183489T>G , CM000673.1:g.118183489T>G GRCh37
NC_000011.8:g.117688699T>G NCBI36
NG_007383.1:g.13195T>G , LRG_38:g.13195T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.260T>G MANE Select ENSP00000354566.4:p.Phe87Cys
ENST00000361763.8:c.260T>G ENSP00000354566.4:p.Phe87Cys
ENST00000526146.5:n.806T>G
ENST00000528435.5:n.813T>G
ENST00000528600.1:c.242T>G ENSP00000433975.1:p.Phe81Cys
ENST00000529713.5:n.366T>G
ENST00000531913.1:n.631T>G
NM_000733.3:c.260T>G , LRG_38t1:c.260T>G NP_000724.1:p.Phe87Cys
NM_000733.4:c.260T>G MANE Select NP_000724.1:p.Phe87Cys
Search 100 bp 5'
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