Canonical Allele Identifier: CA2003457066
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339869C= , CM000673.2:g.118339869C= GRCh38
NC_000011.9:g.118210584C= , CM000673.1:g.118210584C= GRCh37
NC_000011.8:g.117715794C= NCBI36
NG_007566.1:g.526C= , LRG_39:g.526C=
NG_009891.1:g.7876G= , LRG_37:g.7876G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.799G=
ENST00000695667.1:n.317G=
ENST00000695668.1:n.2297G=
ENST00000300692.9:c.312G= MANE Select ENSP00000300692.4:p.Val104=
ENST00000300692.8:c.312G= ENSP00000300692.4:p.Val104=
ENST00000392884.2:c.275-375G= ENSP00000376622.2:n.275-375G=
ENST00000526561.1:n.80-375G=
ENST00000529594.5:c.93G= ENSP00000437335.1:p.Val31=
ENST00000534687.5:c.288-375G=
NM_000732.4:c.312G= , LRG_37t1:c.312G= NP_000723.1:p.Val104=
NM_001040651.1:c.275-375G= NP_001035741.1:n.275-375G=
NM_001040651.2:c.275-375G= NP_001035741.1:n.275-375G=
NM_000732.6:c.312G= MANE Select NP_000723.1:p.Val104=