Canonical Allele Identifier: CA2697558977

Gene: CD3D

Linked Data

• ClinVar Variation Id: 2704297
• ClinVar RCV Id: RCV003583317

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339761G>A , CM000673.2:g.118339761G>A	GRCh38
NC_000011.9:g.118210476G>A , CM000673.1:g.118210476G>A	GRCh37
NC_000011.8:g.117715686G>A	NCBI36
NG_007566.1:g.418G>A , LRG_39:g.418G>A
NG_009891.1:g.7984C>T , LRG_37:g.7984C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.907C>T
ENST00000695667.1:n.425C>T
ENST00000695668.1:n.2405C>T
ENST00000300692.9:c.406+14C>T MANE Select	ENSP00000300692.4:n.406+14C>T
ENST00000300692.8:c.406+14C>T	ENSP00000300692.4:n.406+14C>T
ENST00000392884.2:c.275-267C>T	ENSP00000376622.2:n.275-267C>T
ENST00000526561.1:n.80-267C>T
ENST00000529594.5:c.187+14C>T	ENSP00000437335.1:n.187+14C>T
ENST00000534687.5:c.288-267C>T
NM_000732.4:c.406+14C>T , LRG_37t1:c.406+14C>T	NP_000723.1:n.406+14C>T
NM_001040651.1:c.275-267C>T	NP_001035741.1:n.275-267C>T
NM_001040651.2:c.275-267C>T	NP_001035741.1:n.275-267C>T
NM_000732.6:c.406+14C>T MANE Select	NP_000723.1:n.406+14C>T