Canonical Allele Identifier: CA2616232391

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339680-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339680A>C , CM000673.2:g.118339680A>C	GRCh38
NC_000011.9:g.118210395A>C , CM000673.1:g.118210395A>C	GRCh37
NC_000011.8:g.117715605A>C	NCBI36
NG_007566.1:g.337A>C , LRG_39:g.337A>C
NG_009891.1:g.8065T>G , LRG_37:g.8065T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.988T>G
ENST00000695667.1:n.506T>G
ENST00000300692.9:c.406+95T>G MANE Select	ENSP00000300692.4:n.406+95T>G
ENST00000300692.8:c.406+95T>G	ENSP00000300692.4:n.406+95T>G
ENST00000392884.2:c.275-186T>G	ENSP00000376622.2:n.275-186T>G
ENST00000526561.1:n.80-186T>G
ENST00000529594.5:c.187+95T>G	ENSP00000437335.1:n.187+95T>G
ENST00000534687.5:c.288-186T>G
NM_000732.4:c.406+95T>G , LRG_37t1:c.406+95T>G	NP_000723.1:n.406+95T>G
NM_001040651.1:c.275-186T>G	NP_001035741.1:n.275-186T>G
NM_001040651.2:c.275-186T>G	NP_001035741.1:n.275-186T>G
NM_000732.6:c.406+95T>G MANE Select	NP_000723.1:n.406+95T>G