Canonical Allele Identifier: CA2574994322

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339880_118339881insC , CM000673.2:g.118339880_118339881insC	GRCh38
NC_000011.9:g.118210595_118210596insC , CM000673.1:g.118210595_118210596insC	GRCh37
NC_000011.8:g.117715805_117715806insC	NCBI36
NG_007566.1:g.537_538insC , LRG_39:g.537_538insC
NG_009891.1:g.7864_7865insG , LRG_37:g.7864_7865insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.787_788insG
ENST00000695667.1:n.305_306insG
ENST00000695668.1:n.2285_2286insG
ENST00000300692.9:c.300_301insG MANE Select	ENSP00000300692.4:p.Pro101AlafsTer11
ENST00000300692.8:c.300_301insG	ENSP00000300692.4:p.Pro101AlafsTer11
ENST00000392884.2:c.275-387_275-386insG	ENSP00000376622.2:n.275-387_275-386insG
ENST00000526561.1:n.80-387_80-386insG
ENST00000529594.5:c.81_82insG	ENSP00000437335.1:p.Pro28AlafsTer11
ENST00000534687.5:c.288-387_288-386insG
NM_000732.4:c.300_301insG , LRG_37t1:c.300_301insG	NP_000723.1:p.Pro101AlafsTer11
NM_001040651.1:c.275-387_275-386insG	NP_001035741.1:n.275-387_275-386insG
NM_001040651.2:c.275-387_275-386insG	NP_001035741.1:n.275-387_275-386insG
NM_000732.6:c.300_301insG MANE Select	NP_000723.1:p.Pro101AlafsTer11