Canonical Allele Identifier: CA2003457032
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339799G= , CM000673.2:g.118339799G= GRCh38
NC_000011.9:g.118210514G= , CM000673.1:g.118210514G= GRCh37
NC_000011.8:g.117715724G= NCBI36
NG_007566.1:g.456G= , LRG_39:g.456G=
NG_009891.1:g.7946C= , LRG_37:g.7946C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.869C=
ENST00000695667.1:n.387C=
ENST00000695668.1:n.2367C=
ENST00000300692.9:c.382C= MANE Select ENSP00000300692.4:p.His128=
ENST00000300692.8:c.382C= ENSP00000300692.4:p.His128=
ENST00000392884.2:c.275-305C= ENSP00000376622.2:n.275-305C=
ENST00000526561.1:n.80-305C=
ENST00000529594.5:c.163C= ENSP00000437335.1:p.His55=
ENST00000534687.5:c.288-305C=
NM_000732.4:c.382C= , LRG_37t1:c.382C= NP_000723.1:p.His128=
NM_001040651.1:c.275-305C= NP_001035741.1:n.275-305C=
NM_001040651.2:c.275-305C= NP_001035741.1:n.275-305C=
NM_000732.6:c.382C= MANE Select NP_000723.1:p.His128=