Canonical Allele Identifier: CA2793810947

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339711_118339717del , CM000673.2:g.118339711_118339717del	GRCh38
NC_000011.9:g.118210426_118210432del , CM000673.1:g.118210426_118210432del	GRCh37
NC_000011.8:g.117715636_117715642del	NCBI36
NG_007566.1:g.368_374del , LRG_39:g.368_374del
NG_009891.1:g.8028_8034del , LRG_37:g.8028_8034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.951_957del
ENST00000695667.1:n.469_475del
ENST00000300692.9:c.406+58_406+64del MANE Select	ENSP00000300692.4:n.406+58_406+64del
ENST00000300692.8:c.406+58_406+64del	ENSP00000300692.4:n.406+58_406+64del
ENST00000392884.2:c.275-223_275-217del	ENSP00000376622.2:n.275-223_275-217del
ENST00000526561.1:n.80-223_80-217del
ENST00000529594.5:c.187+58_187+64del	ENSP00000437335.1:n.187+58_187+64del
ENST00000534687.5:c.288-223_288-217del
NM_000732.4:c.406+58_406+64del , LRG_37t1:c.406+58_406+64del	NP_000723.1:n.406+58_406+64del
NM_001040651.1:c.275-223_275-217del	NP_001035741.1:n.275-223_275-217del
NM_001040651.2:c.275-223_275-217del	NP_001035741.1:n.275-223_275-217del
NM_000732.6:c.406+58_406+64del MANE Select	NP_000723.1:n.406+58_406+64del