Canonical Allele Identifier: CA2616232405

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339706-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339706T>C , CM000673.2:g.118339706T>C	GRCh38
NC_000011.9:g.118210421T>C , CM000673.1:g.118210421T>C	GRCh37
NC_000011.8:g.117715631T>C	NCBI36
NG_007566.1:g.363T>C , LRG_39:g.363T>C
NG_009891.1:g.8039A>G , LRG_37:g.8039A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.962A>G
ENST00000695667.1:n.480A>G
ENST00000300692.9:c.406+69A>G MANE Select	ENSP00000300692.4:n.406+69A>G
ENST00000300692.8:c.406+69A>G	ENSP00000300692.4:n.406+69A>G
ENST00000392884.2:c.275-212A>G	ENSP00000376622.2:n.275-212A>G
ENST00000526561.1:n.80-212A>G
ENST00000529594.5:c.187+69A>G	ENSP00000437335.1:n.187+69A>G
ENST00000534687.5:c.288-212A>G
NM_000732.4:c.406+69A>G , LRG_37t1:c.406+69A>G	NP_000723.1:n.406+69A>G
NM_001040651.1:c.275-212A>G	NP_001035741.1:n.275-212A>G
NM_001040651.2:c.275-212A>G	NP_001035741.1:n.275-212A>G
NM_000732.6:c.406+69A>G MANE Select	NP_000723.1:n.406+69A>G