Canonical Allele Identifier: CA2003457035
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339802C= , CM000673.2:g.118339802C= GRCh38
NC_000011.9:g.118210517C= , CM000673.1:g.118210517C= GRCh37
NC_000011.8:g.117715727C= NCBI36
NG_007566.1:g.459C= , LRG_39:g.459C=
NG_009891.1:g.7943G= , LRG_37:g.7943G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695666.1:n.866G=
ENST00000695667.1:n.384G=
ENST00000695668.1:n.2364G=
ENST00000300692.9:c.379G= MANE Select ENSP00000300692.4:p.Gly127=
ENST00000300692.8:c.379G= ENSP00000300692.4:p.Gly127=
ENST00000392884.2:c.275-308G= ENSP00000376622.2:n.275-308G=
ENST00000526561.1:n.80-308G=
ENST00000529594.5:c.160G= ENSP00000437335.1:p.Gly54=
ENST00000534687.5:c.288-308G=
NM_000732.4:c.379G= , LRG_37t1:c.379G= NP_000723.1:p.Gly127=
NM_001040651.1:c.275-308G= NP_001035741.1:n.275-308G=
NM_001040651.2:c.275-308G= NP_001035741.1:n.275-308G=
NM_000732.6:c.379G= MANE Select NP_000723.1:p.Gly127=