Canonical Allele Identifier: CA2003457101
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339945T= , CM000673.2:g.118339945T= GRCh38
NC_000011.9:g.118210660T= , CM000673.1:g.118210660T= GRCh37
NC_000011.8:g.117715870T= NCBI36
NG_007566.1:g.602T= , LRG_39:g.602T=
NG_009891.1:g.7800A= , LRG_37:g.7800A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.723A=
ENST00000695667.1:n.280-39A=
ENST00000695668.1:n.2260-39A=
ENST00000300692.9:c.275-39A= MANE Select ENSP00000300692.4:n.275-39A=
ENST00000300692.8:c.275-39A= ENSP00000300692.4:n.275-39A=
ENST00000392884.2:c.274+430A= ENSP00000376622.2:n.274+430A=
ENST00000526561.1:n.80-451A=
ENST00000529594.5:c.56-39A= ENSP00000437335.1:n.56-39A=
ENST00000534687.5:c.287+430A=
NM_000732.4:c.275-39A= , LRG_37t1:c.275-39A= NP_000723.1:n.275-39A=
NM_001040651.1:c.274+430A= NP_001035741.1:n.274+430A=
NM_001040651.2:c.274+430A= NP_001035741.1:n.274+430A=
NM_000732.6:c.275-39A= MANE Select NP_000723.1:n.275-39A=