Canonical Allele Identifier: CA2542620044

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059078
• gnomAD v4: 11-118339712-A-ACACT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339715_118339716insTCAC , CM000673.2:g.118339715_118339716insTCAC	GRCh38
NC_000011.9:g.118210430_118210431insTCAC , CM000673.1:g.118210430_118210431insTCAC	GRCh37
NC_000011.8:g.117715640_117715641insTCAC	NCBI36
NG_007566.1:g.372_373insTCAC , LRG_39:g.372_373insTCAC
NG_009891.1:g.8032_8033insAGTG , LRG_37:g.8032_8033insAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.955_956insAGTG
ENST00000695667.1:n.473_474insAGTG
ENST00000300692.9:c.406+62_406+63insAGTG MANE Select	ENSP00000300692.4:n.406+62_406+63insAGTG
ENST00000300692.8:c.406+62_406+63insAGTG	ENSP00000300692.4:n.406+62_406+63insAGTG
ENST00000392884.2:c.275-219_275-218insAGTG	ENSP00000376622.2:n.275-219_275-218insAGTG
ENST00000526561.1:n.80-219_80-218insAGTG
ENST00000529594.5:c.187+62_187+63insAGTG	ENSP00000437335.1:n.187+62_187+63insAGTG
ENST00000534687.5:c.288-219_288-218insAGTG
NM_000732.4:c.406+62_406+63insAGTG , LRG_37t1:c.406+62_406+63insAGTG	NP_000723.1:n.406+62_406+63insAGTG
NM_001040651.1:c.275-219_275-218insAGTG	NP_001035741.1:n.275-219_275-218insAGTG
NM_001040651.2:c.275-219_275-218insAGTG	NP_001035741.1:n.275-219_275-218insAGTG
NM_000732.6:c.406+62_406+63insAGTG MANE Select	NP_000723.1:n.406+62_406+63insAGTG