Canonical Allele Identifier: CA2003457052
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339838T= , CM000673.2:g.118339838T= GRCh38
NC_000011.9:g.118210553T= , CM000673.1:g.118210553T= GRCh37
NC_000011.8:g.117715763T= NCBI36
NG_007566.1:g.495T= , LRG_39:g.495T=
NG_009891.1:g.7907A= , LRG_37:g.7907A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.830A=
ENST00000695667.1:n.348A=
ENST00000695668.1:n.2328A=
ENST00000300692.9:c.343A= MANE Select ENSP00000300692.4:p.Thr115=
ENST00000300692.8:c.343A= ENSP00000300692.4:p.Thr115=
ENST00000392884.2:c.275-344A= ENSP00000376622.2:n.275-344A=
ENST00000526561.1:n.80-344A=
ENST00000529594.5:c.124A= ENSP00000437335.1:p.Thr42=
ENST00000534687.5:c.288-344A=
NM_000732.4:c.343A= , LRG_37t1:c.343A= NP_000723.1:p.Thr115=
NM_001040651.1:c.275-344A= NP_001035741.1:n.275-344A=
NM_001040651.2:c.275-344A= NP_001035741.1:n.275-344A=
NM_000732.6:c.343A= MANE Select NP_000723.1:p.Thr115=