Canonical Allele Identifier: CA2616232422

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339723-C-CACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339726_118339727insTACA , CM000673.2:g.118339726_118339727insTACA	GRCh38
NC_000011.9:g.118210441_118210442insTACA , CM000673.1:g.118210441_118210442insTACA	GRCh37
NC_000011.8:g.117715651_117715652insTACA	NCBI36
NG_007566.1:g.383_384insTACA , LRG_39:g.383_384insTACA
NG_009891.1:g.8021_8022insATGT , LRG_37:g.8021_8022insATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.944_945insATGT
ENST00000695667.1:n.462_463insATGT
ENST00000695668.1:n.2442_2443insATGT
ENST00000300692.9:c.406+51_406+52insATGT MANE Select	ENSP00000300692.4:n.406+51_406+52insATGT
ENST00000300692.8:c.406+51_406+52insATGT	ENSP00000300692.4:n.406+51_406+52insATGT
ENST00000392884.2:c.275-230_275-229insATGT	ENSP00000376622.2:n.275-230_275-229insATGT
ENST00000526561.1:n.80-230_80-229insATGT
ENST00000529594.5:c.187+51_187+52insATGT	ENSP00000437335.1:n.187+51_187+52insATGT
ENST00000534687.5:c.288-230_288-229insATGT
NM_000732.4:c.406+51_406+52insATGT , LRG_37t1:c.406+51_406+52insATGT	NP_000723.1:n.406+51_406+52insATGT
NM_001040651.1:c.275-230_275-229insATGT	NP_001035741.1:n.275-230_275-229insATGT
NM_001040651.2:c.275-230_275-229insATGT	NP_001035741.1:n.275-230_275-229insATGT
NM_000732.6:c.406+51_406+52insATGT MANE Select	NP_000723.1:n.406+51_406+52insATGT