Canonical Allele Identifier: CA2003457195
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340194T= , CM000673.2:g.118340194T= GRCh38
NC_000011.9:g.118210909T= , CM000673.1:g.118210909T= GRCh37
NC_000011.8:g.117716119T= NCBI36
NG_007566.1:g.851T= , LRG_39:g.851T=
NG_009891.1:g.7551A= , LRG_37:g.7551A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.474A=
ENST00000695667.1:n.279+181A=
ENST00000695668.1:n.2259+181A=
ENST00000300692.9:c.274+181A= MANE Select ENSP00000300692.4:n.274+181A=
ENST00000300692.8:c.274+181A= ENSP00000300692.4:n.274+181A=
ENST00000392884.2:c.274+181A= ENSP00000376622.2:n.274+181A=
ENST00000526561.1:n.80-700A=
ENST00000529594.5:c.56-288A= ENSP00000437335.1:n.56-288A=
ENST00000534687.5:c.287+181A=
NM_000732.4:c.274+181A= , LRG_37t1:c.274+181A= NP_000723.1:n.274+181A=
NM_001040651.1:c.274+181A= NP_001035741.1:n.274+181A=
NM_001040651.2:c.274+181A= NP_001035741.1:n.274+181A=
NM_000732.6:c.274+181A= MANE Select NP_000723.1:n.274+181A=