Canonical Allele Identifier: CA2003457134
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340025C= , CM000673.2:g.118340025C= GRCh38
NC_000011.9:g.118210740C= , CM000673.1:g.118210740C= GRCh37
NC_000011.8:g.117715950C= NCBI36
NG_007566.1:g.682C= , LRG_39:g.682C=
NG_009891.1:g.7720G= , LRG_37:g.7720G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.643G=
ENST00000695667.1:n.280-119G=
ENST00000695668.1:n.2260-119G=
ENST00000300692.9:c.275-119G= MANE Select ENSP00000300692.4:n.275-119G=
ENST00000300692.8:c.275-119G= ENSP00000300692.4:n.275-119G=
ENST00000392884.2:c.274+350G= ENSP00000376622.2:n.274+350G=
ENST00000526561.1:n.80-531G=
ENST00000529594.5:c.56-119G= ENSP00000437335.1:n.56-119G=
ENST00000534687.5:c.287+350G=
NM_000732.4:c.275-119G= , LRG_37t1:c.275-119G= NP_000723.1:n.275-119G=
NM_001040651.1:c.274+350G= NP_001035741.1:n.274+350G=
NM_001040651.2:c.274+350G= NP_001035741.1:n.274+350G=
NM_000732.6:c.275-119G= MANE Select NP_000723.1:n.275-119G=