Canonical Allele Identifier: CA382782047
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183413A>G (hg19) chr11:g.118312698A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312698A>G , CM000673.2:g.118312698A>G GRCh38
NC_000011.9:g.118183413A>G , CM000673.1:g.118183413A>G GRCh37
NC_000011.8:g.117688623A>G NCBI36
NG_007383.1:g.13119A>G , LRG_38:g.13119A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.184A>G MANE Select ENSP00000354566.4:p.Asn62Asp
ENST00000361763.8:c.184A>G ENSP00000354566.4:p.Asn62Asp
ENST00000526146.5:n.730A>G
ENST00000528435.5:n.737A>G
ENST00000528600.1:c.166A>G ENSP00000433975.1:p.Asn56Asp
ENST00000529713.5:n.290A>G
ENST00000531913.1:n.555A>G
NM_000733.3:c.184A>G , LRG_38t1:c.184A>G NP_000724.1:p.Asn62Asp
NM_000733.4:c.184A>G MANE Select NP_000724.1:p.Asn62Asp
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