Canonical Allele Identifier: CA2725025487
Gene: CD3D HGNC NCBI

Linked Data

dbSNP Id: rs2134059114

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339720_118339721insTACA , CM000673.2:g.118339720_118339721insTACA GRCh38
NC_000011.9:g.118210435_118210436insTACA , CM000673.1:g.118210435_118210436insTACA GRCh37
NC_000011.8:g.117715645_117715646insTACA NCBI36
NG_007566.1:g.377_378insTACA , LRG_39:g.377_378insTACA
NG_009891.1:g.8027_8028insATGT , LRG_37:g.8027_8028insATGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.950_951insATGT
ENST00000695667.1:n.468_469insATGT
ENST00000300692.9:c.406+57_406+58insATGT MANE Select ENSP00000300692.4:n.406+57_406+58insATGT
ENST00000300692.8:c.406+57_406+58insATGT ENSP00000300692.4:n.406+57_406+58insATGT
ENST00000392884.2:c.275-224_275-223insATGT ENSP00000376622.2:n.275-224_275-223insATGT
ENST00000526561.1:n.80-224_80-223insATGT
ENST00000529594.5:c.187+57_187+58insATGT ENSP00000437335.1:n.187+57_187+58insATGT
ENST00000534687.5:c.288-224_288-223insATGT
NM_000732.4:c.406+57_406+58insATGT , LRG_37t1:c.406+57_406+58insATGT NP_000723.1:n.406+57_406+58insATGT
NM_001040651.1:c.275-224_275-223insATGT NP_001035741.1:n.275-224_275-223insATGT
NM_001040651.2:c.275-224_275-223insATGT NP_001035741.1:n.275-224_275-223insATGT
NM_000732.6:c.406+57_406+58insATGT MANE Select NP_000723.1:n.406+57_406+58insATGT