Canonical Allele Identifier: CA2003457187
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340180C= , CM000673.2:g.118340180C= GRCh38
NC_000011.9:g.118210895C= , CM000673.1:g.118210895C= GRCh37
NC_000011.8:g.117716105C= NCBI36
NG_007566.1:g.837C= , LRG_39:g.837C=
NG_009891.1:g.7565G= , LRG_37:g.7565G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.488G=
ENST00000695667.1:n.279+195G=
ENST00000695668.1:n.2259+195G=
ENST00000300692.9:c.274+195G= MANE Select ENSP00000300692.4:n.274+195G=
ENST00000300692.8:c.274+195G= ENSP00000300692.4:n.274+195G=
ENST00000392884.2:c.274+195G= ENSP00000376622.2:n.274+195G=
ENST00000526561.1:n.80-686G=
ENST00000529594.5:c.56-274G= ENSP00000437335.1:n.56-274G=
ENST00000534687.5:c.287+195G=
NM_000732.4:c.274+195G= , LRG_37t1:c.274+195G= NP_000723.1:n.274+195G=
NM_001040651.1:c.274+195G= NP_001035741.1:n.274+195G=
NM_001040651.2:c.274+195G= NP_001035741.1:n.274+195G=
NM_000732.6:c.274+195G= MANE Select NP_000723.1:n.274+195G=