Canonical Allele Identifier: CA1794116356
Gene: GDAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74364082A= , CM000670.2:g.74364082A= GRCh38
NC_000008.10:g.75276317A= , CM000670.1:g.75276317A= GRCh37
NC_000008.9:g.75438872A= NCBI36
NG_008787.2:g.47953A=
NG_008787.3:g.47953A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220822.12:c.792A= MANE Select ENSP00000220822.7:p.Ala264=
ENST00000434412.3:c.660A= ENSP00000417006.3:p.Ala220=
ENST00000520797.6:n.903A=
ENST00000521096.6:n.648A=
ENST00000522568.2:c.*464A= ENSP00000430136.1:n.*464A=
ENST00000523640.2:c.165+12761A= ENSP00000502017.1:n.165+12761A=
ENST00000524195.2:c.280+1029A= ENSP00000502308.1:n.280+1029A=
ENST00000674612.1:c.465A= ENSP00000501864.1:p.Ala155=
ENST00000674710.1:c.694+1029A= ENSP00000502762.1:n.694+1029A=
ENST00000674754.1:c.*2355A= ENSP00000502063.1:n.*2355A=
ENST00000674756.1:c.*366+1029A= ENSP00000501860.1:n.*366+1029A=
ENST00000674806.1:c.465A= ENSP00000502637.1:p.Ala155=
ENST00000674865.1:c.588A= ENSP00000502437.1:p.Ala196=
ENST00000674926.1:c.*1424A= ENSP00000501799.1:n.*1424A=
ENST00000674934.1:c.*480A= ENSP00000502187.1:n.*480A=
ENST00000674944.1:c.*1395A= ENSP00000501858.1:n.*1395A=
ENST00000674946.1:c.694+1029A= ENSP00000501569.1:n.694+1029A=
ENST00000674973.1:c.486A= ENSP00000502447.1:p.Ala162=
ENST00000675007.1:c.*530A= ENSP00000502119.1:n.*530A=
ENST00000675060.1:c.*457A= ENSP00000501616.1:n.*457A=
ENST00000675165.1:c.789A= ENSP00000502612.1:p.Ala263=
ENST00000675220.1:c.465A= ENSP00000502588.1:p.Ala155=
ENST00000675265.1:c.*542A= ENSP00000501848.1:n.*542A=
ENST00000675336.1:c.*278A= ENSP00000502120.1:n.*278A=
ENST00000675376.1:c.465A= ENSP00000502838.1:p.Ala155=
ENST00000675463.1:c.870A= ENSP00000502327.1:p.Ala290=
ENST00000675472.1:c.*278A= ENSP00000501946.1:n.*278A=
ENST00000675474.1:n.377A=
ENST00000675560.1:c.*366+1029A= ENSP00000502118.1:n.*366+1029A=
ENST00000675625.1:c.*464A= ENSP00000501626.1:n.*464A=
ENST00000675633.1:c.*199A= ENSP00000501785.1:n.*199A=
ENST00000675661.1:c.*552A= ENSP00000501958.1:n.*552A=
ENST00000675706.1:n.2750A=
ENST00000675821.1:c.465A= ENSP00000502198.1:p.Ala155=
ENST00000675832.1:c.*464A= ENSP00000502041.1:n.*464A=
ENST00000675928.1:c.618A= ENSP00000501568.1:p.Ala206=
ENST00000675944.1:c.588A= ENSP00000502673.1:p.Ala196=
ENST00000675999.1:c.694+1029A= ENSP00000502572.1:n.694+1029A=
ENST00000676049.1:c.*694A= ENSP00000501912.1:n.*694A=
ENST00000676112.1:c.858A= ENSP00000502295.1:p.Ala286=
ENST00000676143.1:c.465A= ENSP00000502828.1:p.Ala155=
ENST00000676207.1:c.694+1029A= ENSP00000502638.1:n.694+1029A=
ENST00000676377.1:c.465A= ENSP00000502756.1:p.Ala155=
ENST00000676415.1:c.*98A= ENSP00000502665.1:n.*98A=
ENST00000676443.1:c.744A= ENSP00000501769.1:p.Ala248=
ENST00000220822.11:c.792A= ENSP00000220822.7:p.Ala264=
ENST00000434412.2:c.588A= ENSP00000417006.2:p.Ala196=
ENST00000520797.5:n.557A=
ENST00000521096.5:n.598A=
ENST00000522568.1:c.*464A= ENSP00000430136.1:n.*464A=
ENST00000524195.1:n.103+1029A=
NM_001040875.2:c.588A= NP_001035808.1:p.Ala196=
NM_018972.2:c.792A= NP_061845.2:p.Ala264=
NR_046346.1:n.726A=
XM_011517551.1:c.1086A= XP_011515853.1:p.Ala362=
XM_011517552.1:c.465A= XP_011515854.1:p.Ala155=
NM_001040875.3:c.588A= NP_001035808.1:p.Ala196=
NM_001362929.1:c.465A= NP_001349858.1:p.Ala155=
NM_001362930.1:c.618A= NP_001349859.1:p.Ala206=
NM_001362931.1:c.694+1029A= NP_001349860.1:n.694+1029A=
NM_001362932.1:c.465A= NP_001349861.1:p.Ala155=
NM_018972.3:c.792A= NP_061845.2:p.Ala264=
NM_001362931.2:c.694+1029A= NP_001349860.1:n.694+1029A=
NM_018972.4:c.792A= MANE Select NP_061845.2:p.Ala264=
NM_001040875.4:c.588A= NP_001035808.1:p.Ala196=
NM_001362929.2:c.465A= NP_001349858.1:p.Ala155=
NM_001362930.2:c.618A= NP_001349859.1:p.Ala206=
NM_001362932.2:c.465A= NP_001349861.1:p.Ala155=