Canonical Allele Identifier: CA2616232406
Gene: CD3D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339708_118339711del , CM000673.2:g.118339708_118339711del GRCh38
NC_000011.9:g.118210423_118210426del , CM000673.1:g.118210423_118210426del GRCh37
NC_000011.8:g.117715633_117715636del NCBI36
NG_007566.1:g.365_368del , LRG_39:g.365_368del
NG_009891.1:g.8034_8037del , LRG_37:g.8034_8037del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.957_960del
ENST00000695667.1:n.475_478del
ENST00000300692.9:c.406+64_406+67del MANE Select ENSP00000300692.4:n.406+64_406+67del
ENST00000300692.8:c.406+64_406+67del ENSP00000300692.4:n.406+64_406+67del
ENST00000392884.2:c.275-217_275-214del ENSP00000376622.2:n.275-217_275-214del
ENST00000526561.1:n.80-217_80-214del
ENST00000529594.5:c.187+64_187+67del ENSP00000437335.1:n.187+64_187+67del
ENST00000534687.5:c.288-217_288-214del
NM_000732.4:c.406+64_406+67del , LRG_37t1:c.406+64_406+67del NP_000723.1:n.406+64_406+67del
NM_001040651.1:c.275-217_275-214del NP_001035741.1:n.275-217_275-214del
NM_001040651.2:c.275-217_275-214del NP_001035741.1:n.275-217_275-214del
NM_000732.6:c.406+64_406+67del MANE Select NP_000723.1:n.406+64_406+67del