Canonical Allele Identifier: CA2003457074
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339902G= , CM000673.2:g.118339902G= GRCh38
NC_000011.9:g.118210617G= , CM000673.1:g.118210617G= GRCh37
NC_000011.8:g.117715827G= NCBI36
NG_007566.1:g.559G= , LRG_39:g.559G=
NG_009891.1:g.7843C= , LRG_37:g.7843C=

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.279C= MANE Select NP_000723.1:p.Cys93=
ENST00000300692.9:c.279C= MANE Select ENSP00000300692.4:p.Cys93=
NM_000732.4:c.279C= , LRG_37t1:c.279C= NP_000723.1:p.Cys93=
NM_001040651.1:c.275-408C= NP_001035741.1:n.275-408C=
NM_001040651.2:c.275-408C= NP_001035741.1:n.275-408C=
ENST00000300692.8:c.279C= ENSP00000300692.4:p.Cys93=
ENST00000392884.2:c.275-408C= ENSP00000376622.2:n.275-408C=
ENST00000526561.1:n.80-408C=
ENST00000529594.5:c.60C= ENSP00000437335.1:p.Cys20=
ENST00000534687.5:c.288-408C=
ENST00000695666.1:n.766C=
ENST00000695667.1:n.284C=
ENST00000695668.1:n.2264C=