Canonical Allele Identifier: CA2003457182
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340171G= , CM000673.2:g.118340171G= GRCh38
NC_000011.9:g.118210886G= , CM000673.1:g.118210886G= GRCh37
NC_000011.8:g.117716096G= NCBI36
NG_007566.1:g.828G= , LRG_39:g.828G=
NG_009891.1:g.7574C= , LRG_37:g.7574C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.497C=
ENST00000695667.1:n.279+204C=
ENST00000695668.1:n.2259+204C=
ENST00000300692.9:c.274+204C= MANE Select ENSP00000300692.4:n.274+204C=
ENST00000300692.8:c.274+204C= ENSP00000300692.4:n.274+204C=
ENST00000392884.2:c.274+204C= ENSP00000376622.2:n.274+204C=
ENST00000526561.1:n.80-677C=
ENST00000529594.5:c.56-265C= ENSP00000437335.1:n.56-265C=
ENST00000534687.5:c.287+204C=
NM_000732.4:c.274+204C= , LRG_37t1:c.274+204C= NP_000723.1:n.274+204C=
NM_001040651.1:c.274+204C= NP_001035741.1:n.274+204C=
NM_001040651.2:c.274+204C= NP_001035741.1:n.274+204C=
NM_000732.6:c.274+204C= MANE Select NP_000723.1:n.274+204C=