Canonical Allele Identifier: CA371550180
Gene: GDAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74364067G>C , CM000670.2:g.74364067G>C GRCh38
NC_000008.10:g.75276302G>C , CM000670.1:g.75276302G>C GRCh37
NC_000008.9:g.75438857G>C NCBI36
NG_008787.2:g.47938G>C
NG_008787.3:g.47938G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220822.12:c.777G>C MANE Select ENSP00000220822.7:p.Lys259Asn
ENST00000434412.3:c.645G>C ENSP00000417006.3:p.Lys215Asn
ENST00000520797.6:n.888G>C
ENST00000521096.6:n.633G>C
ENST00000522568.2:c.*449G>C ENSP00000430136.1:n.*449G>C
ENST00000523640.2:c.165+12746G>C ENSP00000502017.1:n.165+12746G>C
ENST00000524195.2:c.280+1014G>C ENSP00000502308.1:n.280+1014G>C
ENST00000674612.1:c.450G>C ENSP00000501864.1:p.Lys150Asn
ENST00000674710.1:c.694+1014G>C ENSP00000502762.1:n.694+1014G>C
ENST00000674754.1:c.*2340G>C ENSP00000502063.1:n.*2340G>C
ENST00000674756.1:c.*366+1014G>C ENSP00000501860.1:n.*366+1014G>C
ENST00000674806.1:c.450G>C ENSP00000502637.1:p.Lys150Asn
ENST00000674865.1:c.573G>C ENSP00000502437.1:p.Lys191Asn
ENST00000674926.1:c.*1409G>C ENSP00000501799.1:n.*1409G>C
ENST00000674934.1:c.*465G>C ENSP00000502187.1:n.*465G>C
ENST00000674944.1:c.*1380G>C ENSP00000501858.1:n.*1380G>C
ENST00000674946.1:c.694+1014G>C ENSP00000501569.1:n.694+1014G>C
ENST00000674973.1:c.471G>C ENSP00000502447.1:p.Lys157Asn
ENST00000675007.1:c.*515G>C ENSP00000502119.1:n.*515G>C
ENST00000675060.1:c.*442G>C ENSP00000501616.1:n.*442G>C
ENST00000675165.1:c.774G>C ENSP00000502612.1:p.Lys258Asn
ENST00000675220.1:c.450G>C ENSP00000502588.1:p.Lys150Asn
ENST00000675265.1:c.*527G>C ENSP00000501848.1:n.*527G>C
ENST00000675336.1:c.*263G>C ENSP00000502120.1:n.*263G>C
ENST00000675376.1:c.450G>C ENSP00000502838.1:p.Lys150Asn
ENST00000675463.1:c.855G>C ENSP00000502327.1:p.Lys285Asn
ENST00000675472.1:c.*263G>C ENSP00000501946.1:n.*263G>C
ENST00000675474.1:n.362G>C
ENST00000675560.1:c.*366+1014G>C ENSP00000502118.1:n.*366+1014G>C
ENST00000675625.1:c.*449G>C ENSP00000501626.1:n.*449G>C
ENST00000675633.1:c.*184G>C ENSP00000501785.1:n.*184G>C
ENST00000675661.1:c.*537G>C ENSP00000501958.1:n.*537G>C
ENST00000675706.1:n.2735G>C
ENST00000675821.1:c.450G>C ENSP00000502198.1:p.Lys150Asn
ENST00000675832.1:c.*449G>C ENSP00000502041.1:n.*449G>C
ENST00000675928.1:c.603G>C ENSP00000501568.1:p.Lys201Asn
ENST00000675944.1:c.573G>C ENSP00000502673.1:p.Lys191Asn
ENST00000675999.1:c.694+1014G>C ENSP00000502572.1:n.694+1014G>C
ENST00000676049.1:c.*679G>C ENSP00000501912.1:n.*679G>C
ENST00000676112.1:c.843G>C ENSP00000502295.1:p.Lys281Asn
ENST00000676143.1:c.450G>C ENSP00000502828.1:p.Lys150Asn
ENST00000676207.1:c.694+1014G>C ENSP00000502638.1:n.694+1014G>C
ENST00000676377.1:c.450G>C ENSP00000502756.1:p.Lys150Asn
ENST00000676415.1:c.*83G>C ENSP00000502665.1:n.*83G>C
ENST00000676443.1:c.729G>C ENSP00000501769.1:p.Lys243Asn
ENST00000220822.11:c.777G>C ENSP00000220822.7:p.Lys259Asn
ENST00000434412.2:c.573G>C ENSP00000417006.2:p.Lys191Asn
ENST00000520797.5:n.542G>C
ENST00000521096.5:n.583G>C
ENST00000522568.1:c.*449G>C ENSP00000430136.1:n.*449G>C
ENST00000524195.1:n.103+1014G>C
NM_001040875.2:c.573G>C NP_001035808.1:p.Lys191Asn
NM_018972.2:c.777G>C NP_061845.2:p.Lys259Asn
NR_046346.1:n.711G>C
XM_011517551.1:c.1071G>C XP_011515853.1:p.Lys357Asn
XM_011517552.1:c.450G>C XP_011515854.1:p.Lys150Asn
NM_001040875.3:c.573G>C NP_001035808.1:p.Lys191Asn
NM_001362929.1:c.450G>C NP_001349858.1:p.Lys150Asn
NM_001362930.1:c.603G>C NP_001349859.1:p.Lys201Asn
NM_001362931.1:c.694+1014G>C NP_001349860.1:n.694+1014G>C
NM_001362932.1:c.450G>C NP_001349861.1:p.Lys150Asn
NM_018972.3:c.777G>C NP_061845.2:p.Lys259Asn
NM_001362931.2:c.694+1014G>C NP_001349860.1:n.694+1014G>C
NM_018972.4:c.777G>C MANE Select NP_061845.2:p.Lys259Asn
NM_001040875.4:c.573G>C NP_001035808.1:p.Lys191Asn
NM_001362929.2:c.450G>C NP_001349858.1:p.Lys150Asn
NM_001362930.2:c.603G>C NP_001349859.1:p.Lys201Asn
NM_001362932.2:c.450G>C NP_001349861.1:p.Lys150Asn