Canonical Allele Identifier: CA229522102
Community Standard Title: NM_000732.6(CD3D):c.440A>G (p.Gln147Arg)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339461T>C , CM000673.2:g.118339461T>C GRCh38
NC_000011.9:g.118210176T>C , CM000673.1:g.118210176T>C GRCh37
NC_000011.8:g.117715386T>C NCBI36
NG_007566.1:g.118T>C , LRG_39:g.118T>C
NG_009891.1:g.8284A>G , LRG_37:g.8284A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.440A>G MANE Select NP_000723.1:p.Gln147Arg
ENST00000300692.9:c.440A>G MANE Select ENSP00000300692.4:p.Gln147Arg
NM_000732.4:c.440A>G , LRG_37t1:c.440A>G NP_000723.1:p.Gln147Arg
NM_001040651.1:c.308A>G NP_001035741.1:p.Gln103Arg
NM_001040651.2:c.308A>G NP_001035741.1:p.Gln103Arg
ENST00000300692.8:c.440A>G ENSP00000300692.4:p.Gln147Arg
ENST00000392884.2:c.308A>G ENSP00000376622.2:p.Gln103Arg
ENST00000526561.1:n.113A>G
ENST00000529594.5:c.221A>G ENSP00000437335.1:p.Gln74Arg
ENST00000534687.5:c.321A>G
ENST00000695666.1:n.1207A>G
ENST00000695667.1:n.725A>G