Canonical Allele Identifier: CA2003457036
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339803A= , CM000673.2:g.118339803A= GRCh38
NC_000011.9:g.118210518A= , CM000673.1:g.118210518A= GRCh37
NC_000011.8:g.117715728A= NCBI36
NG_007566.1:g.460A= , LRG_39:g.460A=
NG_009891.1:g.7942T= , LRG_37:g.7942T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695666.1:n.865T=
ENST00000695667.1:n.383T=
ENST00000695668.1:n.2363T=
ENST00000300692.9:c.378T= MANE Select ENSP00000300692.4:p.Ala126=
ENST00000300692.8:c.378T= ENSP00000300692.4:p.Ala126=
ENST00000392884.2:c.275-309T= ENSP00000376622.2:n.275-309T=
ENST00000526561.1:n.80-309T=
ENST00000529594.5:c.159T= ENSP00000437335.1:p.Ala53=
ENST00000534687.5:c.288-309T=
NM_000732.4:c.378T= , LRG_37t1:c.378T= NP_000723.1:p.Ala126=
NM_001040651.1:c.275-309T= NP_001035741.1:n.275-309T=
NM_001040651.2:c.275-309T= NP_001035741.1:n.275-309T=
NM_000732.6:c.378T= MANE Select NP_000723.1:p.Ala126=