Canonical Allele Identifier: CA1794116493
Gene: GDAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74364159A= , CM000670.2:g.74364159A= GRCh38
NC_000008.10:g.75276394A= , CM000670.1:g.75276394A= GRCh37
NC_000008.9:g.75438949A= NCBI36
NG_008787.2:g.48030A=
NG_008787.3:g.48030A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220822.12:c.869A= MANE Select ENSP00000220822.7:p.Asn290=
ENST00000434412.3:c.737A= ENSP00000417006.3:p.Asn246=
ENST00000520797.6:n.980A=
ENST00000521096.6:n.725A=
ENST00000522568.2:c.*541A= ENSP00000430136.1:n.*541A=
ENST00000523640.2:c.165+12838A= ENSP00000502017.1:n.165+12838A=
ENST00000524195.2:c.280+1106A= ENSP00000502308.1:n.280+1106A=
ENST00000674612.1:c.542A= ENSP00000501864.1:p.Asn181=
ENST00000674710.1:c.694+1106A= ENSP00000502762.1:n.694+1106A=
ENST00000674754.1:c.*2432A= ENSP00000502063.1:n.*2432A=
ENST00000674756.1:c.*366+1106A= ENSP00000501860.1:n.*366+1106A=
ENST00000674806.1:c.542A= ENSP00000502637.1:p.Asn181=
ENST00000674865.1:c.665A= ENSP00000502437.1:p.Asn222=
ENST00000674926.1:c.*1501A= ENSP00000501799.1:n.*1501A=
ENST00000674934.1:c.*557A= ENSP00000502187.1:n.*557A=
ENST00000674944.1:c.*1472A= ENSP00000501858.1:n.*1472A=
ENST00000674946.1:c.694+1106A= ENSP00000501569.1:n.694+1106A=
ENST00000674973.1:c.563A= ENSP00000502447.1:p.Asn188=
ENST00000675007.1:c.*607A= ENSP00000502119.1:n.*607A=
ENST00000675060.1:c.*534A= ENSP00000501616.1:n.*534A=
ENST00000675165.1:c.866A= ENSP00000502612.1:p.Asn289=
ENST00000675220.1:c.542A= ENSP00000502588.1:p.Asn181=
ENST00000675265.1:c.*619A= ENSP00000501848.1:n.*619A=
ENST00000675336.1:c.*355A= ENSP00000502120.1:n.*355A=
ENST00000675376.1:c.542A= ENSP00000502838.1:p.Asn181=
ENST00000675463.1:c.947A= ENSP00000502327.1:p.Asn316=
ENST00000675472.1:c.*355A= ENSP00000501946.1:n.*355A=
ENST00000675474.1:n.454A=
ENST00000675560.1:c.*366+1106A= ENSP00000502118.1:n.*366+1106A=
ENST00000675625.1:c.*541A= ENSP00000501626.1:n.*541A=
ENST00000675633.1:c.*276A= ENSP00000501785.1:n.*276A=
ENST00000675661.1:c.*629A= ENSP00000501958.1:n.*629A=
ENST00000675706.1:n.2827A=
ENST00000675821.1:c.542A= ENSP00000502198.1:p.Asn181=
ENST00000675832.1:c.*541A= ENSP00000502041.1:n.*541A=
ENST00000675928.1:c.695A= ENSP00000501568.1:p.Asn232=
ENST00000675944.1:c.665A= ENSP00000502673.1:p.Asn222=
ENST00000675999.1:c.694+1106A= ENSP00000502572.1:n.694+1106A=
ENST00000676049.1:c.*771A= ENSP00000501912.1:n.*771A=
ENST00000676112.1:c.935A= ENSP00000502295.1:p.Asn312=
ENST00000676143.1:c.542A= ENSP00000502828.1:p.Asn181=
ENST00000676207.1:c.694+1106A= ENSP00000502638.1:n.694+1106A=
ENST00000676377.1:c.542A= ENSP00000502756.1:p.Asn181=
ENST00000676415.1:c.*175A= ENSP00000502665.1:n.*175A=
ENST00000676443.1:c.821A= ENSP00000501769.1:p.Asn274=
ENST00000220822.11:c.869A= ENSP00000220822.7:p.Asn290=
ENST00000434412.2:c.665A= ENSP00000417006.2:p.Asn222=
ENST00000520797.5:n.634A=
ENST00000521096.5:n.675A=
ENST00000522568.1:c.*541A= ENSP00000430136.1:n.*541A=
ENST00000524195.1:n.103+1106A=
NM_001040875.2:c.665A= NP_001035808.1:p.Asn222=
NM_018972.2:c.869A= NP_061845.2:p.Asn290=
NR_046346.1:n.803A=
XM_011517551.1:c.1163A= XP_011515853.1:p.Asn388=
XM_011517552.1:c.542A= XP_011515854.1:p.Asn181=
NM_001040875.3:c.665A= NP_001035808.1:p.Asn222=
NM_001362929.1:c.542A= NP_001349858.1:p.Asn181=
NM_001362930.1:c.695A= NP_001349859.1:p.Asn232=
NM_001362931.1:c.694+1106A= NP_001349860.1:n.694+1106A=
NM_001362932.1:c.542A= NP_001349861.1:p.Asn181=
NM_018972.3:c.869A= NP_061845.2:p.Asn290=
NM_001362931.2:c.694+1106A= NP_001349860.1:n.694+1106A=
NM_018972.4:c.869A= MANE Select NP_061845.2:p.Asn290=
NM_001040875.4:c.665A= NP_001035808.1:p.Asn222=
NM_001362929.2:c.542A= NP_001349858.1:p.Asn181=
NM_001362930.2:c.695A= NP_001349859.1:p.Asn232=
NM_001362932.2:c.542A= NP_001349861.1:p.Asn181=