Canonical Allele Identifier: CA6302107
Gene: CD3G HGNC NCBI

Linked Data

dbSNP Id: rs778205349

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118349769_118349772del , CM000673.2:g.118349769_118349772del GRCh38
NC_000011.9:g.118220484_118220487del , CM000673.1:g.118220484_118220487del GRCh37
NC_000011.8:g.117725694_117725697del NCBI36
NG_007566.1:g.10426_10429del , LRG_39:g.10426_10429del

Transcript Alleles

HGVS Amino-acid change
ENST00000532917.3:c.106_109del MANE Select ENSP00000431445.2:p.Tyr36LysfsTer8
ENST00000292144.8:c.*163_*166del ENSP00000292144.4:n.*163_*166del
ENST00000392883.6:c.-75_-72del ENSP00000376621.2:n.-75_-72del
ENST00000527777.5:n.186_189del
ENST00000528540.5:n.127_130del
ENST00000532903.1:n.182_185del
ENST00000532917.1:c.106_109del ENSP00000431445.1:p.Tyr36LysfsTer8
ENST00000533462.5:n.878_881del
NM_000073.2:c.106_109del , LRG_39t1:c.106_109del NP_000064.1:p.Tyr36LysfsTer8
XM_005271724.2:c.106_109del XP_005271781.1:p.Tyr36LysfsTer8
XM_006718941.2:c.106_109del XP_006719004.1:p.Tyr36LysfsTer8
XM_005271724.4:c.106_109del XP_005271781.1:p.Tyr36LysfsTer8
XM_006718941.3:c.106_109del XP_006719004.1:p.Tyr36LysfsTer8
NM_000073.3:c.106_109del MANE Select NP_000064.1:p.Tyr36LysfsTer8