Canonical Allele Identifier: CA2003457041
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339810C= , CM000673.2:g.118339810C= GRCh38
NC_000011.9:g.118210525C= , CM000673.1:g.118210525C= GRCh37
NC_000011.8:g.117715735C= NCBI36
NG_007566.1:g.467C= , LRG_39:g.467C=
NG_009891.1:g.7935G= , LRG_37:g.7935G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695666.1:n.858G=
ENST00000695667.1:n.376G=
ENST00000695668.1:n.2356G=
ENST00000300692.9:c.371G= MANE Select ENSP00000300692.4:p.Cys124=
ENST00000300692.8:c.371G= ENSP00000300692.4:p.Cys124=
ENST00000392884.2:c.275-316G= ENSP00000376622.2:n.275-316G=
ENST00000526561.1:n.80-316G=
ENST00000529594.5:c.152G= ENSP00000437335.1:p.Cys51=
ENST00000534687.5:c.288-316G=
NM_000732.4:c.371G= , LRG_37t1:c.371G= NP_000723.1:p.Cys124=
NM_001040651.1:c.275-316G= NP_001035741.1:n.275-316G=
NM_001040651.2:c.275-316G= NP_001035741.1:n.275-316G=
NM_000732.6:c.371G= MANE Select NP_000723.1:p.Cys124=