Canonical Allele Identifier: CA382789084
Community Standard Title: NM_000732.6(CD3D):c.239A>G (p.Lys80Arg)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340410T>C , CM000673.2:g.118340410T>C GRCh38
NC_000011.9:g.118211125T>C , CM000673.1:g.118211125T>C GRCh37
NC_000011.8:g.117716335T>C NCBI36
NG_007566.1:g.1067T>C , LRG_39:g.1067T>C
NG_009891.1:g.7335A>G , LRG_37:g.7335A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.239A>G MANE Select NP_000723.1:p.Lys80Arg
ENST00000300692.9:c.239A>G MANE Select ENSP00000300692.4:p.Lys80Arg
NM_000732.4:c.239A>G , LRG_37t1:c.239A>G NP_000723.1:p.Lys80Arg
NM_001040651.1:c.239A>G NP_001035741.1:p.Lys80Arg
NM_001040651.2:c.239A>G NP_001035741.1:p.Lys80Arg
ENST00000300692.8:c.239A>G ENSP00000300692.4:p.Lys80Arg
ENST00000392884.2:c.239A>G ENSP00000376622.2:p.Lys80Arg
ENST00000526561.1:n.80-916A>G
ENST00000529594.5:c.56-504A>G ENSP00000437335.1:n.56-504A>G
ENST00000534687.5:c.252A>G
ENST00000695666.1:n.258A>G
ENST00000695667.1:n.244A>G
ENST00000695668.1:n.2224A>G