Canonical Allele Identifier: CA2003457058
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339851A= , CM000673.2:g.118339851A= GRCh38
NC_000011.9:g.118210566A= , CM000673.1:g.118210566A= GRCh37
NC_000011.8:g.117715776A= NCBI36
NG_007566.1:g.508A= , LRG_39:g.508A=
NG_009891.1:g.7894T= , LRG_37:g.7894T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.817T=
ENST00000695667.1:n.335T=
ENST00000695668.1:n.2315T=
ENST00000300692.9:c.330T= MANE Select ENSP00000300692.4:p.Thr110=
ENST00000300692.8:c.330T= ENSP00000300692.4:p.Thr110=
ENST00000392884.2:c.275-357T= ENSP00000376622.2:n.275-357T=
ENST00000526561.1:n.80-357T=
ENST00000529594.5:c.111T= ENSP00000437335.1:p.Thr37=
ENST00000534687.5:c.288-357T=
NM_000732.4:c.330T= , LRG_37t1:c.330T= NP_000723.1:p.Thr110=
NM_001040651.1:c.275-357T= NP_001035741.1:n.275-357T=
NM_001040651.2:c.275-357T= NP_001035741.1:n.275-357T=
NM_000732.6:c.330T= MANE Select NP_000723.1:p.Thr110=