Canonical Allele Identifier: CA2793810957
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339723C>A , CM000673.2:g.118339723C>A GRCh38
NC_000011.9:g.118210438C>A , CM000673.1:g.118210438C>A GRCh37
NC_000011.8:g.117715648C>A NCBI36
NG_007566.1:g.380C>A , LRG_39:g.380C>A
NG_009891.1:g.8022G>T , LRG_37:g.8022G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.945G>T
ENST00000695667.1:n.463G>T
ENST00000695668.1:n.2443G>T
ENST00000300692.9:c.406+52G>T MANE Select ENSP00000300692.4:n.406+52G>T
ENST00000300692.8:c.406+52G>T ENSP00000300692.4:n.406+52G>T
ENST00000392884.2:c.275-229G>T ENSP00000376622.2:n.275-229G>T
ENST00000526561.1:n.80-229G>T
ENST00000529594.5:c.187+52G>T ENSP00000437335.1:n.187+52G>T
ENST00000534687.5:c.288-229G>T
NM_000732.4:c.406+52G>T , LRG_37t1:c.406+52G>T NP_000723.1:n.406+52G>T
NM_001040651.1:c.275-229G>T NP_001035741.1:n.275-229G>T
NM_001040651.2:c.275-229G>T NP_001035741.1:n.275-229G>T
NM_000732.6:c.406+52G>T MANE Select NP_000723.1:n.406+52G>T