Canonical Allele Identifier: CA382781933

Gene: CD3E

Linked Data

• gnomAD v4: 11-118312677-T-A
• MyVariant Identifiers: chr11:g.118183392T>A (hg19) ; chr11:g.118312677T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118312677T>A , CM000673.2:g.118312677T>A	GRCh38
NC_000011.9:g.118183392T>A , CM000673.1:g.118183392T>A	GRCh37
NC_000011.8:g.117688602T>A	NCBI36
NG_007383.1:g.13098T>A , LRG_38:g.13098T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361763.9:c.163T>A MANE Select	ENSP00000354566.4:p.Ser55Thr
ENST00000361763.8:c.163T>A	ENSP00000354566.4:p.Ser55Thr
ENST00000526146.5:n.709T>A
ENST00000528435.5:n.716T>A
ENST00000528600.1:c.145T>A	ENSP00000433975.1:p.Ser49Thr
ENST00000529713.5:n.269T>A
ENST00000531913.1:n.534T>A
NM_000733.3:c.163T>A , LRG_38t1:c.163T>A	NP_000724.1:p.Ser55Thr
NM_000733.4:c.163T>A MANE Select	NP_000724.1:p.Ser55Thr