Canonical Allele Identifier: CA6301959
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340371G>A , CM000673.2:g.118340371G>A GRCh38
NC_000011.9:g.118211086G>A , CM000673.1:g.118211086G>A GRCh37
NC_000011.8:g.117716296G>A NCBI36
NG_007566.1:g.1028G>A , LRG_39:g.1028G>A
NG_009891.1:g.7374C>T , LRG_37:g.7374C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.297C>T
ENST00000695667.1:n.279+4C>T
ENST00000695668.1:n.2259+4C>T
ENST00000300692.9:c.274+4C>T MANE Select ENSP00000300692.4:n.274+4C>T
ENST00000300692.8:c.274+4C>T ENSP00000300692.4:n.274+4C>T
ENST00000392884.2:c.274+4C>T ENSP00000376622.2:n.274+4C>T
ENST00000526561.1:n.80-877C>T
ENST00000529594.5:c.56-465C>T ENSP00000437335.1:n.56-465C>T
ENST00000534687.5:c.287+4C>T
NM_000732.4:c.274+4C>T , LRG_37t1:c.274+4C>T NP_000723.1:n.274+4C>T
NM_001040651.1:c.274+4C>T NP_001035741.1:n.274+4C>T
NM_001040651.2:c.274+4C>T NP_001035741.1:n.274+4C>T
NM_000732.6:c.274+4C>T MANE Select NP_000723.1:n.274+4C>T