Canonical Allele Identifier: CA1794116141
Gene: GDAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74363966T= , CM000670.2:g.74363966T= GRCh38
NC_000008.10:g.75276201T= , CM000670.1:g.75276201T= GRCh37
NC_000008.9:g.75438756T= NCBI36
NG_008787.2:g.47837T=
NG_008787.3:g.47837T=

Transcript Alleles

HGVS Amino-acid change
ENST00000220822.12:c.695-19T= MANE Select ENSP00000220822.7:n.695-19T=
ENST00000434412.3:c.563-19T= ENSP00000417006.3:n.563-19T=
ENST00000520797.6:n.806-19T=
ENST00000521096.6:n.551-19T=
ENST00000522568.2:c.*367-19T= ENSP00000430136.1:n.*367-19T=
ENST00000523640.2:c.165+12645T= ENSP00000502017.1:n.165+12645T=
ENST00000524195.2:c.280+913T= ENSP00000502308.1:n.280+913T=
ENST00000674612.1:c.368-19T= ENSP00000501864.1:n.368-19T=
ENST00000674710.1:c.694+913T= ENSP00000502762.1:n.694+913T=
ENST00000674754.1:c.*2239T= ENSP00000502063.1:n.*2239T=
ENST00000674756.1:c.*366+913T= ENSP00000501860.1:n.*366+913T=
ENST00000674806.1:c.368-19T= ENSP00000502637.1:n.368-19T=
ENST00000674865.1:c.491-19T= ENSP00000502437.1:n.491-19T=
ENST00000674926.1:c.*1327-19T= ENSP00000501799.1:n.*1327-19T=
ENST00000674934.1:c.*383-19T= ENSP00000502187.1:n.*383-19T=
ENST00000674944.1:c.*1279T= ENSP00000501858.1:n.*1279T=
ENST00000674946.1:c.694+913T= ENSP00000501569.1:n.694+913T=
ENST00000674973.1:c.389-19T= ENSP00000502447.1:n.389-19T=
ENST00000675007.1:c.*433-19T= ENSP00000502119.1:n.*433-19T=
ENST00000675060.1:c.*360-19T= ENSP00000501616.1:n.*360-19T=
ENST00000675165.1:c.695-22T= ENSP00000502612.1:n.695-22T=
ENST00000675220.1:c.368-19T= ENSP00000502588.1:n.368-19T=
ENST00000675265.1:c.*445-19T= ENSP00000501848.1:n.*445-19T=
ENST00000675336.1:c.*181-19T= ENSP00000502120.1:n.*181-19T=
ENST00000675376.1:c.368-19T= ENSP00000502838.1:n.368-19T=
ENST00000675463.1:c.773-19T= ENSP00000502327.1:n.773-19T=
ENST00000675472.1:c.*181-19T= ENSP00000501946.1:n.*181-19T=
ENST00000675474.1:n.280-19T=
ENST00000675560.1:c.*366+913T= ENSP00000502118.1:n.*366+913T=
ENST00000675625.1:c.*367-19T= ENSP00000501626.1:n.*367-19T=
ENST00000675633.1:c.*102-19T= ENSP00000501785.1:n.*102-19T=
ENST00000675661.1:c.*455-19T= ENSP00000501958.1:n.*455-19T=
ENST00000675706.1:n.2634T=
ENST00000675821.1:c.368-19T= ENSP00000502198.1:n.368-19T=
ENST00000675832.1:c.*367-19T= ENSP00000502041.1:n.*367-19T=
ENST00000675928.1:c.521-19T= ENSP00000501568.1:n.521-19T=
ENST00000675944.1:c.491-19T= ENSP00000502673.1:n.491-19T=
ENST00000675999.1:c.694+913T= ENSP00000502572.1:n.694+913T=
ENST00000676049.1:c.*597-19T= ENSP00000501912.1:n.*597-19T=
ENST00000676112.1:c.761-19T= ENSP00000502295.1:n.761-19T=
ENST00000676143.1:c.368-19T= ENSP00000502828.1:n.368-19T=
ENST00000676207.1:c.694+913T= ENSP00000502638.1:n.694+913T=
ENST00000676377.1:c.368-19T= ENSP00000502756.1:n.368-19T=
ENST00000676415.1:c.717T= ENSP00000502665.1:p.Tyr239=
ENST00000676443.1:c.647-19T= ENSP00000501769.1:n.647-19T=
ENST00000220822.11:c.695-19T= ENSP00000220822.7:n.695-19T=
ENST00000434412.2:c.491-19T= ENSP00000417006.2:n.491-19T=
ENST00000520797.5:n.460-19T=
ENST00000521096.5:n.501-19T=
ENST00000522568.1:c.*367-19T= ENSP00000430136.1:n.*367-19T=
ENST00000524195.1:n.103+913T=
ENST00000524366.5:n.539-19T=
NM_001040875.2:c.491-19T= NP_001035808.1:n.491-19T=
NM_018972.2:c.695-19T= NP_061845.2:n.695-19T=
NR_046346.1:n.629-19T=
XM_011517551.1:c.989-19T= XP_011515853.1:n.989-19T=
XM_011517552.1:c.368-19T= XP_011515854.1:n.368-19T=
NM_001040875.3:c.491-19T= NP_001035808.1:n.491-19T=
NM_001362929.1:c.368-19T= NP_001349858.1:n.368-19T=
NM_001362930.1:c.521-19T= NP_001349859.1:n.521-19T=
NM_001362931.1:c.694+913T= NP_001349860.1:n.694+913T=
NM_001362932.1:c.368-19T= NP_001349861.1:n.368-19T=
NM_018972.3:c.695-19T= NP_061845.2:n.695-19T=
NM_001362931.2:c.694+913T= NP_001349860.1:n.694+913T=
NM_018972.4:c.695-19T= MANE Select NP_061845.2:n.695-19T=
NM_001040875.4:c.491-19T= NP_001035808.1:n.491-19T=
NM_001362929.2:c.368-19T= NP_001349858.1:n.368-19T=
NM_001362930.2:c.521-19T= NP_001349859.1:n.521-19T=
NM_001362932.2:c.368-19T= NP_001349861.1:n.368-19T=