Canonical Allele Identifier: CA6301622
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs750597143
ExAC: 11:118183299 GTTTCTTCTGCCAA / G
gnomAD v2: 11-118183299-GTTTCTTCTGCCAA-G
gnomAD v3: 11-118312584-GTTTCTTCTGCCAA-G
gnomAD v4: 11-118312584-GTTTCTTCTGCCAA-G
MyVariant Identifiers: chr11:g.118183300_118183312del (hg19) chr11:g.118312586_118312598del (hg38) chr11:g.118312585_118312597del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312589_118312601del , CM000673.2:g.118312589_118312601del GRCh38
NC_000011.9:g.118183304_118183316del , CM000673.1:g.118183304_118183316del GRCh37
NC_000011.8:g.117688514_117688526del NCBI36
NG_007383.1:g.13010_13022del , LRG_38:g.13010_13022del

Transcript Alleles

HGVS Amino-acid change
ENST00000361763.9:c.104-29_104-17del MANE Select ENSP00000354566.4:n.104-29_104-17del
ENST00000361763.8:c.104-29_104-17del ENSP00000354566.4:n.104-29_104-17del
ENST00000526146.5:n.621_633del
ENST00000528435.5:n.628_640del
ENST00000528600.1:c.86-29_86-17del ENSP00000433975.1:n.86-29_86-17del
ENST00000529713.5:n.210-29_210-17del
ENST00000531913.1:n.446_458del
NM_000733.3:c.104-29_104-17del , LRG_38t1:c.104-29_104-17del NP_000724.1:n.104-29_104-17del
NM_000733.4:c.104-29_104-17del MANE Select NP_000724.1:n.104-29_104-17del
Search 100 bp 5'
Search 100 bp 3'