Canonical Allele Identifier: CA2616232429
Gene: CD3D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339731_118339733del , CM000673.2:g.118339731_118339733del GRCh38
NC_000011.9:g.118210446_118210448del , CM000673.1:g.118210446_118210448del GRCh37
NC_000011.8:g.117715656_117715658del NCBI36
NG_007566.1:g.388_390del , LRG_39:g.388_390del
NG_009891.1:g.8012_8014del , LRG_37:g.8012_8014del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.935_937del
ENST00000695667.1:n.453_455del
ENST00000695668.1:n.2433_2435del
ENST00000300692.9:c.406+42_406+44del MANE Select ENSP00000300692.4:n.406+42_406+44del
ENST00000300692.8:c.406+42_406+44del ENSP00000300692.4:n.406+42_406+44del
ENST00000392884.2:c.275-239_275-237del ENSP00000376622.2:n.275-239_275-237del
ENST00000526561.1:n.80-239_80-237del
ENST00000529594.5:c.187+42_187+44del ENSP00000437335.1:n.187+42_187+44del
ENST00000534687.5:c.288-239_288-237del
NM_000732.4:c.406+42_406+44del , LRG_37t1:c.406+42_406+44del NP_000723.1:n.406+42_406+44del
NM_001040651.1:c.275-239_275-237del NP_001035741.1:n.275-239_275-237del
NM_001040651.2:c.275-239_275-237del NP_001035741.1:n.275-239_275-237del
NM_000732.6:c.406+42_406+44del MANE Select NP_000723.1:n.406+42_406+44del