Canonical Allele Identifier: CA2003457023
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339778C= , CM000673.2:g.118339778C= GRCh38
NC_000011.9:g.118210493C= , CM000673.1:g.118210493C= GRCh37
NC_000011.8:g.117715703C= NCBI36
NG_007566.1:g.435C= , LRG_39:g.435C=
NG_009891.1:g.7967G= , LRG_37:g.7967G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.890G=
ENST00000695667.1:n.408G=
ENST00000695668.1:n.2388G=
ENST00000300692.9:c.403G= MANE Select ENSP00000300692.4:p.Gly135=
ENST00000300692.8:c.403G= ENSP00000300692.4:p.Gly135=
ENST00000392884.2:c.275-284G= ENSP00000376622.2:n.275-284G=
ENST00000526561.1:n.80-284G=
ENST00000529594.5:c.184G= ENSP00000437335.1:p.Gly62=
ENST00000534687.5:c.288-284G=
NM_000732.4:c.403G= , LRG_37t1:c.403G= NP_000723.1:p.Gly135=
NM_001040651.1:c.275-284G= NP_001035741.1:n.275-284G=
NM_001040651.2:c.275-284G= NP_001035741.1:n.275-284G=
NM_000732.6:c.403G= MANE Select NP_000723.1:p.Gly135=