Canonical Allele Identifier: CA382787926
Community Standard Title: NM_000732.6(CD3D):c.418C>G (p.Gln140Glu)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339483G>C , CM000673.2:g.118339483G>C GRCh38
NC_000011.9:g.118210198G>C , CM000673.1:g.118210198G>C GRCh37
NC_000011.8:g.117715408G>C NCBI36
NG_007566.1:g.140G>C , LRG_39:g.140G>C
NG_009891.1:g.8262C>G , LRG_37:g.8262C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.418C>G MANE Select NP_000723.1:p.Gln140Glu
ENST00000300692.9:c.418C>G MANE Select ENSP00000300692.4:p.Gln140Glu
NM_000732.4:c.418C>G , LRG_37t1:c.418C>G NP_000723.1:p.Gln140Glu
NM_001040651.1:c.286C>G NP_001035741.1:p.Gln96Glu
NM_001040651.2:c.286C>G NP_001035741.1:p.Gln96Glu
ENST00000300692.8:c.418C>G ENSP00000300692.4:p.Gln140Glu
ENST00000392884.2:c.286C>G ENSP00000376622.2:p.Gln96Glu
ENST00000526561.1:n.91C>G
ENST00000529594.5:c.199C>G ENSP00000437335.1:p.Gln67Glu
ENST00000534687.5:c.299C>G
ENST00000695666.1:n.1185C>G
ENST00000695667.1:n.703C>G