Canonical Allele Identifier: CA382787794
Community Standard Title: NM_000732.6(CD3D):c.461A>G (p.Asp154Gly)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339217T>C , CM000673.2:g.118339217T>C GRCh38
NC_000011.9:g.118209932T>C , CM000673.1:g.118209932T>C GRCh37
NC_000011.8:g.117715142T>C NCBI36
NG_009891.1:g.8528A>G , LRG_37:g.8528A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.461A>G MANE Select NP_000723.1:p.Asp154Gly
ENST00000300692.9:c.461A>G MANE Select ENSP00000300692.4:p.Asp154Gly
NM_000732.4:c.461A>G , LRG_37t1:c.461A>G NP_000723.1:p.Asp154Gly
NM_001040651.1:c.329A>G NP_001035741.1:p.Asp110Gly
NM_001040651.2:c.329A>G NP_001035741.1:p.Asp110Gly
ENST00000300692.8:c.461A>G ENSP00000300692.4:p.Asp154Gly
ENST00000392884.2:c.329A>G ENSP00000376622.2:p.Asp110Gly
ENST00000526561.1:n.134A>G
ENST00000529594.5:c.242A>G ENSP00000437335.1:p.Asp81Gly
ENST00000534687.5:c.342A>G
ENST00000695666.1:n.1228A>G
ENST00000695667.1:n.746A>G