Canonical Allele Identifier: CA2793810949

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339711_118339712insCC , CM000673.2:g.118339711_118339712insCC	GRCh38
NC_000011.9:g.118210426_118210427insCC , CM000673.1:g.118210426_118210427insCC	GRCh37
NC_000011.8:g.117715636_117715637insCC	NCBI36
NG_007566.1:g.368_369insCC , LRG_39:g.368_369insCC
NG_009891.1:g.8034_8035insGG , LRG_37:g.8034_8035insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.957_958insGG
ENST00000695667.1:n.475_476insGG
ENST00000300692.9:c.406+64_406+65insGG MANE Select	ENSP00000300692.4:n.406+64_406+65insGG
ENST00000300692.8:c.406+64_406+65insGG	ENSP00000300692.4:n.406+64_406+65insGG
ENST00000392884.2:c.275-217_275-216insGG	ENSP00000376622.2:n.275-217_275-216insGG
ENST00000526561.1:n.80-217_80-216insGG
ENST00000529594.5:c.187+64_187+65insGG	ENSP00000437335.1:n.187+64_187+65insGG
ENST00000534687.5:c.288-217_288-216insGG
NM_000732.4:c.406+64_406+65insGG , LRG_37t1:c.406+64_406+65insGG	NP_000723.1:n.406+64_406+65insGG
NM_001040651.1:c.275-217_275-216insGG	NP_001035741.1:n.275-217_275-216insGG
NM_001040651.2:c.275-217_275-216insGG	NP_001035741.1:n.275-217_275-216insGG
NM_000732.6:c.406+64_406+65insGG MANE Select	NP_000723.1:n.406+64_406+65insGG