Canonical Allele Identifier: CA2003457160
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340112C= , CM000673.2:g.118340112C= GRCh38
NC_000011.9:g.118210827C= , CM000673.1:g.118210827C= GRCh37
NC_000011.8:g.117716037C= NCBI36
NG_007566.1:g.769C= , LRG_39:g.769C=
NG_009891.1:g.7633G= , LRG_37:g.7633G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.556G=
ENST00000695667.1:n.280-206G=
ENST00000695668.1:n.2260-206G=
ENST00000300692.9:c.275-206G= MANE Select ENSP00000300692.4:n.275-206G=
ENST00000300692.8:c.275-206G= ENSP00000300692.4:n.275-206G=
ENST00000392884.2:c.274+263G= ENSP00000376622.2:n.274+263G=
ENST00000526561.1:n.80-618G=
ENST00000529594.5:c.56-206G= ENSP00000437335.1:n.56-206G=
ENST00000534687.5:c.287+263G=
NM_000732.4:c.275-206G= , LRG_37t1:c.275-206G= NP_000723.1:n.275-206G=
NM_001040651.1:c.274+263G= NP_001035741.1:n.274+263G=
NM_001040651.2:c.274+263G= NP_001035741.1:n.274+263G=
NM_000732.6:c.275-206G= MANE Select NP_000723.1:n.275-206G=