Canonical Allele Identifier: CA2552466087
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339720A>C , CM000673.2:g.118339720A>C GRCh38
NC_000011.9:g.118210435A>C , CM000673.1:g.118210435A>C GRCh37
NC_000011.8:g.117715645A>C NCBI36
NG_007566.1:g.377A>C , LRG_39:g.377A>C
NG_009891.1:g.8025T>G , LRG_37:g.8025T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.948T>G
ENST00000695667.1:n.466T>G
ENST00000300692.9:c.406+55T>G MANE Select ENSP00000300692.4:n.406+55T>G
ENST00000300692.8:c.406+55T>G ENSP00000300692.4:n.406+55T>G
ENST00000392884.2:c.275-226T>G ENSP00000376622.2:n.275-226T>G
ENST00000526561.1:n.80-226T>G
ENST00000529594.5:c.187+55T>G ENSP00000437335.1:n.187+55T>G
ENST00000534687.5:c.288-226T>G
NM_000732.4:c.406+55T>G , LRG_37t1:c.406+55T>G NP_000723.1:n.406+55T>G
NM_001040651.1:c.275-226T>G NP_001035741.1:n.275-226T>G
NM_001040651.2:c.275-226T>G NP_001035741.1:n.275-226T>G
NM_000732.6:c.406+55T>G MANE Select NP_000723.1:n.406+55T>G