Canonical Allele Identifier: CA2003457070
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339882T= , CM000673.2:g.118339882T= GRCh38
NC_000011.9:g.118210597T= , CM000673.1:g.118210597T= GRCh37
NC_000011.8:g.117715807T= NCBI36
NG_007566.1:g.539T= , LRG_39:g.539T=
NG_009891.1:g.7863A= , LRG_37:g.7863A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.786A=
ENST00000695667.1:n.304A=
ENST00000695668.1:n.2284A=
ENST00000300692.9:c.299A= MANE Select ENSP00000300692.4:p.Asp100=
ENST00000300692.8:c.299A= ENSP00000300692.4:p.Asp100=
ENST00000392884.2:c.275-388A= ENSP00000376622.2:n.275-388A=
ENST00000526561.1:n.80-388A=
ENST00000529594.5:c.80A= ENSP00000437335.1:p.Asp27=
ENST00000534687.5:c.288-388A=
NM_000732.4:c.299A= , LRG_37t1:c.299A= NP_000723.1:p.Asp100=
NM_001040651.1:c.275-388A= NP_001035741.1:n.275-388A=
NM_001040651.2:c.275-388A= NP_001035741.1:n.275-388A=
NM_000732.6:c.299A= MANE Select NP_000723.1:p.Asp100=