Canonical Allele Identifier: CA654536516

Gene: CD3D

Linked Data

• COSMIC: COSN24905841

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118340045T>C , CM000673.2:g.118340045T>C	GRCh38
NC_000011.9:g.118210760T>C , CM000673.1:g.118210760T>C	GRCh37
NC_000011.8:g.117715970T>C	NCBI36
NG_007566.1:g.702T>C , LRG_39:g.702T>C
NG_009891.1:g.7700A>G , LRG_37:g.7700A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.623A>G
ENST00000695667.1:n.280-139A>G
ENST00000695668.1:n.2260-139A>G
ENST00000300692.9:c.275-139A>G MANE Select	ENSP00000300692.4:n.275-139A>G
ENST00000300692.8:c.275-139A>G	ENSP00000300692.4:n.275-139A>G
ENST00000392884.2:c.274+330A>G	ENSP00000376622.2:n.274+330A>G
ENST00000526561.1:n.80-551A>G
ENST00000529594.5:c.56-139A>G	ENSP00000437335.1:n.56-139A>G
ENST00000534687.5:c.287+330A>G
NM_000732.4:c.275-139A>G , LRG_37t1:c.275-139A>G	NP_000723.1:n.275-139A>G
NM_001040651.1:c.274+330A>G	NP_001035741.1:n.274+330A>G
NM_001040651.2:c.274+330A>G	NP_001035741.1:n.274+330A>G
NM_000732.6:c.275-139A>G MANE Select	NP_000723.1:n.275-139A>G