Canonical Allele Identifier: CA1115359116
Gene: GDAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1809382633

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74361899_74361900del , CM000670.2:g.74361899_74361900del GRCh38
NC_000008.10:g.75274134_75274135del , CM000670.1:g.75274134_75274135del GRCh37
NC_000008.9:g.75436689_75436690del NCBI36
NG_008787.2:g.45770_45771del
NG_008787.3:g.45770_45771del

Transcript Alleles

HGVS Amino-acid change
ENST00000220822.12:c.500_501del MANE Select ENSP00000220822.7:p.Thr167ArgfsTer3
ENST00000434412.3:c.368_369del ENSP00000417006.3:p.Thr123ArgfsTer3
ENST00000520797.6:n.611_612del
ENST00000521096.6:n.356_357del
ENST00000522568.2:c.*172_*173del ENSP00000430136.1:n.*172_*173del
ENST00000523640.2:c.165+10578_165+10579del ENSP00000502017.1:n.165+10578_165+10579de...
ENST00000524195.2:c.166-1040_166-1039del ENSP00000502308.1:n.166-1040_166-1039del
ENST00000674612.1:c.173_174del ENSP00000501864.1:p.Thr58ArgfsTer3
ENST00000674710.1:c.500_501del ENSP00000502762.1:p.Thr167ArgfsTer3
ENST00000674754.1:c.*172_*173del ENSP00000502063.1:n.*172_*173del
ENST00000674756.1:c.*172_*173del ENSP00000501860.1:n.*172_*173del
ENST00000674806.1:c.173_174del ENSP00000502637.1:p.Thr58ArgfsTer3
ENST00000674865.1:c.296_297del ENSP00000502437.1:p.Thr99ArgfsTer3
ENST00000674926.1:c.*172_*173del ENSP00000501799.1:n.*172_*173del
ENST00000674934.1:c.*188_*189del ENSP00000502187.1:n.*188_*189del
ENST00000674944.1:c.*172_*173del ENSP00000501858.1:n.*172_*173del
ENST00000674946.1:c.500_501del ENSP00000501569.1:p.Thr167ArgfsTer3
ENST00000674973.1:c.194_195del ENSP00000502447.1:p.Thr65ArgfsTer3
ENST00000675007.1:c.*172_*173del ENSP00000502119.1:n.*172_*173del
ENST00000675060.1:c.*165_*166del ENSP00000501616.1:n.*165_*166del
ENST00000675165.1:c.500_501del ENSP00000502612.1:p.Thr167ArgfsTer3
ENST00000675220.1:c.173_174del ENSP00000502588.1:p.Thr58ArgfsTer3
ENST00000675265.1:c.*172_*173del ENSP00000501848.1:n.*172_*173del
ENST00000675336.1:c.181_182del ENSP00000502120.1:p.Gln61GlufsTer?
ENST00000675376.1:c.173_174del ENSP00000502838.1:p.Thr58ArgfsTer3
ENST00000675463.1:c.500_501del ENSP00000502327.1:p.Thr167ArgfsTer3
ENST00000675472.1:c.133_134del ENSP00000501946.1:p.Gln45GlufsTer?
ENST00000675560.1:c.*172_*173del ENSP00000502118.1:n.*172_*173del
ENST00000675565.1:n.317_318del
ENST00000675625.1:c.*172_*173del ENSP00000501626.1:n.*172_*173del
ENST00000675633.1:c.500_501del ENSP00000501785.1:p.Thr167ArgfsTer3
ENST00000675661.1:c.*172_*173del ENSP00000501958.1:n.*172_*173del
ENST00000675706.1:n.567_568del
ENST00000675821.1:c.173_174del ENSP00000502198.1:p.Thr58ArgfsTer3
ENST00000675832.1:c.*172_*173del ENSP00000502041.1:n.*172_*173del
ENST00000675928.1:c.326_327del ENSP00000501568.1:p.Thr109ArgfsTer3
ENST00000675944.1:c.296_297del ENSP00000502673.1:p.Thr99ArgfsTer3
ENST00000675999.1:c.500_501del ENSP00000502572.1:p.Thr167ArgfsTer3
ENST00000676049.1:c.*402_*403del ENSP00000501912.1:n.*402_*403del
ENST00000676112.1:c.500_501del ENSP00000502295.1:p.Thr167ArgfsTer3
ENST00000676120.1:c.*172_*173del ENSP00000502036.1:n.*172_*173del
ENST00000676143.1:c.173_174del ENSP00000502828.1:p.Thr58ArgfsTer3
ENST00000676207.1:c.500_501del ENSP00000502638.1:p.Thr167ArgfsTer3
ENST00000676377.1:c.173_174del ENSP00000502756.1:p.Thr58ArgfsTer3
ENST00000676415.1:c.500_501del ENSP00000502665.1:p.Thr167ArgfsTer3
ENST00000676443.1:c.452_453del ENSP00000501769.1:p.Thr151ArgfsTer3
ENST00000220822.11:c.500_501del ENSP00000220822.7:p.Thr167ArgfsTer3
ENST00000434412.2:c.296_297del ENSP00000417006.2:p.Thr99ArgfsTer3
ENST00000520797.5:n.265_266del
ENST00000521096.5:n.306_307del
ENST00000522568.1:c.*172_*173del ENSP00000430136.1:n.*172_*173del
ENST00000524366.5:n.344_345del
NM_001040875.2:c.296_297del NP_001035808.1:p.Thr99ArgfsTer3
NM_018972.2:c.500_501del NP_061845.2:p.Thr167ArgfsTer3
NR_046346.1:n.434_435del
XM_011517551.1:c.794_795del XP_011515853.1:p.Thr265ArgfsTer3
XM_011517552.1:c.173_174del XP_011515854.1:p.Thr58ArgfsTer3
NM_001040875.3:c.296_297del NP_001035808.1:p.Thr99ArgfsTer3
NM_001362929.1:c.173_174del NP_001349858.1:p.Thr58ArgfsTer3
NM_001362930.1:c.326_327del NP_001349859.1:p.Thr109ArgfsTer3
NM_001362931.1:c.500_501del NP_001349860.1:p.Thr167ArgfsTer3
NM_001362932.1:c.173_174del NP_001349861.1:p.Thr58ArgfsTer3
NM_018972.3:c.500_501del NP_061845.2:p.Thr167ArgfsTer3
XM_017013586.2:c.500_501del XP_016869075.2:p.Thr167ArgfsTer3
NM_001362931.2:c.500_501del NP_001349860.1:p.Thr167ArgfsTer3
NM_018972.4:c.500_501del MANE Select NP_061845.2:p.Thr167ArgfsTer3
NM_001040875.4:c.296_297del NP_001035808.1:p.Thr99ArgfsTer3
NM_001362929.2:c.173_174del NP_001349858.1:p.Thr58ArgfsTer3
NM_001362930.2:c.326_327del NP_001349859.1:p.Thr109ArgfsTer3
NM_001362932.2:c.173_174del NP_001349861.1:p.Thr58ArgfsTer3