Canonical Allele Identifier: CA2003457031
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339795T= , CM000673.2:g.118339795T= GRCh38
NC_000011.9:g.118210510T= , CM000673.1:g.118210510T= GRCh37
NC_000011.8:g.117715720T= NCBI36
NG_007566.1:g.452T= , LRG_39:g.452T=
NG_009891.1:g.7950A= , LRG_37:g.7950A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.873A=
ENST00000695667.1:n.391A=
ENST00000695668.1:n.2371A=
ENST00000300692.9:c.386A= MANE Select ENSP00000300692.4:p.Glu129=
ENST00000300692.8:c.386A= ENSP00000300692.4:p.Glu129=
ENST00000392884.2:c.275-301A= ENSP00000376622.2:n.275-301A=
ENST00000526561.1:n.80-301A=
ENST00000529594.5:c.167A= ENSP00000437335.1:p.Glu56=
ENST00000534687.5:c.288-301A=
NM_000732.4:c.386A= , LRG_37t1:c.386A= NP_000723.1:p.Glu129=
NM_001040651.1:c.275-301A= NP_001035741.1:n.275-301A=
NM_001040651.2:c.275-301A= NP_001035741.1:n.275-301A=
NM_000732.6:c.386A= MANE Select NP_000723.1:p.Glu129=