Canonical Allele Identifier: CA2739271719

Gene: CD3D

Linked Data

• ClinVar Variation Id: 2838513
• ClinVar RCV Id: RCV003744404

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339763T>C , CM000673.2:g.118339763T>C	GRCh38
NC_000011.9:g.118210478T>C , CM000673.1:g.118210478T>C	GRCh37
NC_000011.8:g.117715688T>C	NCBI36
NG_007566.1:g.420T>C , LRG_39:g.420T>C
NG_009891.1:g.7982A>G , LRG_37:g.7982A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.905A>G
ENST00000695667.1:n.423A>G
ENST00000695668.1:n.2403A>G
ENST00000300692.9:c.406+12A>G MANE Select	ENSP00000300692.4:n.406+12A>G
ENST00000300692.8:c.406+12A>G	ENSP00000300692.4:n.406+12A>G
ENST00000392884.2:c.275-269A>G	ENSP00000376622.2:n.275-269A>G
ENST00000526561.1:n.80-269A>G
ENST00000529594.5:c.187+12A>G	ENSP00000437335.1:n.187+12A>G
ENST00000534687.5:c.288-269A>G
NM_000732.4:c.406+12A>G , LRG_37t1:c.406+12A>G	NP_000723.1:n.406+12A>G
NM_001040651.1:c.275-269A>G	NP_001035741.1:n.275-269A>G
NM_001040651.2:c.275-269A>G	NP_001035741.1:n.275-269A>G
NM_000732.6:c.406+12A>G MANE Select	NP_000723.1:n.406+12A>G