Canonical Allele Identifier: CA2003456971
Gene: CD3D HGNC NCBI

Linked Data

dbSNP Id: rs1948282315

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339730_118339731insTACACA , CM000673.2:g.118339730_118339731insTACACA GRCh38
NC_000011.9:g.118210445_118210446insTACACA , CM000673.1:g.118210445_118210446insTACACA GRCh37
NC_000011.8:g.117715655_117715656insTACACA NCBI36
NG_007566.1:g.387_388insTACACA , LRG_39:g.387_388insTACACA
NG_009891.1:g.8019_8020insATGTGT , LRG_37:g.8019_8020insATGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.942_943insATGTGT
ENST00000695667.1:n.460_461insATGTGT
ENST00000695668.1:n.2440_2441insATGTGT
ENST00000300692.9:c.406+49_406+50insATGTGT MANE Select ENSP00000300692.4:n.406+49_406+50insATGTGT
ENST00000300692.8:c.406+49_406+50insATGTGT ENSP00000300692.4:n.406+49_406+50insATGTGT
ENST00000392884.2:c.275-232_275-231insATGTGT ENSP00000376622.2:n.275-232_275-231insATGTGT
ENST00000526561.1:n.80-232_80-231insATGTGT
ENST00000529594.5:c.187+49_187+50insATGTGT ENSP00000437335.1:n.187+49_187+50insATGTGT
ENST00000534687.5:c.288-232_288-231insATGTGT
NM_000732.4:c.406+49_406+50insATGTGT , LRG_37t1:c.406+49_406+50insATGTGT NP_000723.1:n.406+49_406+50insATGTGT
NM_001040651.1:c.275-232_275-231insATGTGT NP_001035741.1:n.275-232_275-231insATGTGT
NM_001040651.2:c.275-232_275-231insATGTGT NP_001035741.1:n.275-232_275-231insATGTGT
NM_000732.6:c.406+49_406+50insATGTGT MANE Select NP_000723.1:n.406+49_406+50insATGTGT