Canonical Allele Identifier: CA2565970052
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339919G>T , CM000673.2:g.118339919G>T GRCh38
NC_000011.9:g.118210634G>T , CM000673.1:g.118210634G>T GRCh37
NC_000011.8:g.117715844G>T NCBI36
NG_007566.1:g.576G>T , LRG_39:g.576G>T
NG_009891.1:g.7826C>A , LRG_37:g.7826C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695666.1:n.749C>A
ENST00000695667.1:n.280-13C>A
ENST00000695668.1:n.2260-13C>A
ENST00000300692.9:c.275-13C>A MANE Select ENSP00000300692.4:n.275-13C>A
ENST00000300692.8:c.275-13C>A ENSP00000300692.4:n.275-13C>A
ENST00000392884.2:c.275-425C>A ENSP00000376622.2:n.275-425C>A
ENST00000526561.1:n.80-425C>A
ENST00000529594.5:c.56-13C>A ENSP00000437335.1:n.56-13C>A
ENST00000534687.5:c.288-425C>A
NM_000732.4:c.275-13C>A , LRG_37t1:c.275-13C>A NP_000723.1:n.275-13C>A
NM_001040651.1:c.275-425C>A NP_001035741.1:n.275-425C>A
NM_001040651.2:c.275-425C>A NP_001035741.1:n.275-425C>A
NM_000732.6:c.275-13C>A MANE Select NP_000723.1:n.275-13C>A