Canonical Allele Identifier: CA2616232449
Gene: CD3D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339915del , CM000673.2:g.118339915del GRCh38
NC_000011.9:g.118210630del , CM000673.1:g.118210630del GRCh37
NC_000011.8:g.117715840del NCBI36
NG_007566.1:g.572del , LRG_39:g.572del
NG_009891.1:g.7834del , LRG_37:g.7834del

Transcript Alleles

HGVS Amino-acid change
ENST00000695666.1:n.757del
ENST00000695667.1:n.280-5del
ENST00000695668.1:n.2260-5del
ENST00000300692.9:c.275-5del MANE Select ENSP00000300692.4:n.275-5del
ENST00000300692.8:c.275-5del ENSP00000300692.4:n.275-5del
ENST00000392884.2:c.275-417del ENSP00000376622.2:n.275-417del
ENST00000526561.1:n.80-417del
ENST00000529594.5:c.56-5del ENSP00000437335.1:n.56-5del
ENST00000534687.5:c.288-417del
NM_000732.4:c.275-5del , LRG_37t1:c.275-5del NP_000723.1:n.275-5del
NM_001040651.1:c.275-417del NP_001035741.1:n.275-417del
NM_001040651.2:c.275-417del NP_001035741.1:n.275-417del
NM_000732.6:c.275-5del MANE Select NP_000723.1:n.275-5del