Canonical Allele Identifier: CA2003457161
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340119T= , CM000673.2:g.118340119T= GRCh38
NC_000011.9:g.118210834T= , CM000673.1:g.118210834T= GRCh37
NC_000011.8:g.117716044T= NCBI36
NG_007566.1:g.776T= , LRG_39:g.776T=
NG_009891.1:g.7626A= , LRG_37:g.7626A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.549A=
ENST00000695667.1:n.280-213A=
ENST00000695668.1:n.2260-213A=
ENST00000300692.9:c.275-213A= MANE Select ENSP00000300692.4:n.275-213A=
ENST00000300692.8:c.275-213A= ENSP00000300692.4:n.275-213A=
ENST00000392884.2:c.274+256A= ENSP00000376622.2:n.274+256A=
ENST00000526561.1:n.80-625A=
ENST00000529594.5:c.56-213A= ENSP00000437335.1:n.56-213A=
ENST00000534687.5:c.287+256A=
NM_000732.4:c.275-213A= , LRG_37t1:c.275-213A= NP_000723.1:n.275-213A=
NM_001040651.1:c.274+256A= NP_001035741.1:n.274+256A=
NM_001040651.2:c.274+256A= NP_001035741.1:n.274+256A=
NM_000732.6:c.275-213A= MANE Select NP_000723.1:n.275-213A=