Canonical Allele Identifier: CA2003457089
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339935G= , CM000673.2:g.118339935G= GRCh38
NC_000011.9:g.118210650G= , CM000673.1:g.118210650G= GRCh37
NC_000011.8:g.117715860G= NCBI36
NG_007566.1:g.592G= , LRG_39:g.592G=
NG_009891.1:g.7810C= , LRG_37:g.7810C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.733C=
ENST00000695667.1:n.280-29C=
ENST00000695668.1:n.2260-29C=
ENST00000300692.9:c.275-29C= MANE Select ENSP00000300692.4:n.275-29C=
ENST00000300692.8:c.275-29C= ENSP00000300692.4:n.275-29C=
ENST00000392884.2:c.275-441C= ENSP00000376622.2:n.275-441C=
ENST00000526561.1:n.80-441C=
ENST00000529594.5:c.56-29C= ENSP00000437335.1:n.56-29C=
ENST00000534687.5:c.288-441C=
NM_000732.4:c.275-29C= , LRG_37t1:c.275-29C= NP_000723.1:n.275-29C=
NM_001040651.1:c.275-441C= NP_001035741.1:n.275-441C=
NM_001040651.2:c.275-441C= NP_001035741.1:n.275-441C=
NM_000732.6:c.275-29C= MANE Select NP_000723.1:n.275-29C=