Canonical Allele Identifier: CA2725025779

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059145

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339730_118339731insTACA , CM000673.2:g.118339730_118339731insTACA	GRCh38
NC_000011.9:g.118210445_118210446insTACA , CM000673.1:g.118210445_118210446insTACA	GRCh37
NC_000011.8:g.117715655_117715656insTACA	NCBI36
NG_007566.1:g.387_388insTACA , LRG_39:g.387_388insTACA
NG_009891.1:g.8017_8018insATGT , LRG_37:g.8017_8018insATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.940_941insATGT
ENST00000695667.1:n.458_459insATGT
ENST00000695668.1:n.2438_2439insATGT
ENST00000300692.9:c.406+47_406+48insATGT MANE Select	ENSP00000300692.4:n.406+47_406+48insATGT
ENST00000300692.8:c.406+47_406+48insATGT	ENSP00000300692.4:n.406+47_406+48insATGT
ENST00000392884.2:c.275-234_275-233insATGT	ENSP00000376622.2:n.275-234_275-233insATGT
ENST00000526561.1:n.80-234_80-233insATGT
ENST00000529594.5:c.187+47_187+48insATGT	ENSP00000437335.1:n.187+47_187+48insATGT
ENST00000534687.5:c.288-234_288-233insATGT
NM_000732.4:c.406+47_406+48insATGT , LRG_37t1:c.406+47_406+48insATGT	NP_000723.1:n.406+47_406+48insATGT
NM_001040651.1:c.275-234_275-233insATGT	NP_001035741.1:n.275-234_275-233insATGT
NM_001040651.2:c.275-234_275-233insATGT	NP_001035741.1:n.275-234_275-233insATGT
NM_000732.6:c.406+47_406+48insATGT MANE Select	NP_000723.1:n.406+47_406+48insATGT