Canonical Allele Identifier: CA2793810954
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339714del , CM000673.2:g.118339714del GRCh38
NC_000011.9:g.118210429del , CM000673.1:g.118210429del GRCh37
NC_000011.8:g.117715639del NCBI36
NG_007566.1:g.371del , LRG_39:g.371del
NG_009891.1:g.8031del , LRG_37:g.8031del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.954del
ENST00000695667.1:n.472del
ENST00000300692.9:c.406+61del MANE Select ENSP00000300692.4:n.406+61del
ENST00000300692.8:c.406+61del ENSP00000300692.4:n.406+61del
ENST00000392884.2:c.275-220del ENSP00000376622.2:n.275-220del
ENST00000526561.1:n.80-220del
ENST00000529594.5:c.187+61del ENSP00000437335.1:n.187+61del
ENST00000534687.5:c.288-220del
NM_000732.4:c.406+61del , LRG_37t1:c.406+61del NP_000723.1:n.406+61del
NM_001040651.1:c.275-220del NP_001035741.1:n.275-220del
NM_001040651.2:c.275-220del NP_001035741.1:n.275-220del
NM_000732.6:c.406+61del MANE Select NP_000723.1:n.406+61del