Canonical Allele Identifier: CA461772329

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276281T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364046T>G , CM000670.2:g.74364046T>G	GRCh38
NC_000008.10:g.75276281T>G , CM000670.1:g.75276281T>G	GRCh37
NC_000008.9:g.75438836T>G	NCBI36
NG_008787.2:g.47917T>G
NG_008787.3:g.47917T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000220822.12:c.756T>G MANE Select	ENSP00000220822.7:p.Ala252=
ENST00000434412.3:c.624T>G	ENSP00000417006.3:p.Ala208=
ENST00000520797.6:n.867T>G
ENST00000521096.6:n.612T>G
ENST00000522568.2:c.*428T>G	ENSP00000430136.1:n.*428T>G
ENST00000523640.2:c.165+12725T>G	ENSP00000502017.1:n.165+12725T>G
ENST00000524195.2:c.280+993T>G	ENSP00000502308.1:n.280+993T>G
ENST00000674612.1:c.429T>G	ENSP00000501864.1:p.Ala143=
ENST00000674710.1:c.694+993T>G	ENSP00000502762.1:n.694+993T>G
ENST00000674754.1:c.*2319T>G	ENSP00000502063.1:n.*2319T>G
ENST00000674756.1:c.*366+993T>G	ENSP00000501860.1:n.*366+993T>G
ENST00000674806.1:c.429T>G	ENSP00000502637.1:p.Ala143=
ENST00000674865.1:c.552T>G	ENSP00000502437.1:p.Ala184=
ENST00000674926.1:c.*1388T>G	ENSP00000501799.1:n.*1388T>G
ENST00000674934.1:c.*444T>G	ENSP00000502187.1:n.*444T>G
ENST00000674944.1:c.*1359T>G	ENSP00000501858.1:n.*1359T>G
ENST00000674946.1:c.694+993T>G	ENSP00000501569.1:n.694+993T>G
ENST00000674973.1:c.450T>G	ENSP00000502447.1:p.Ala150=
ENST00000675007.1:c.*494T>G	ENSP00000502119.1:n.*494T>G
ENST00000675060.1:c.*421T>G	ENSP00000501616.1:n.*421T>G
ENST00000675165.1:c.753T>G	ENSP00000502612.1:p.Ala251=
ENST00000675220.1:c.429T>G	ENSP00000502588.1:p.Ala143=
ENST00000675265.1:c.*506T>G	ENSP00000501848.1:n.*506T>G
ENST00000675336.1:c.*242T>G	ENSP00000502120.1:n.*242T>G
ENST00000675376.1:c.429T>G	ENSP00000502838.1:p.Ala143=
ENST00000675463.1:c.834T>G	ENSP00000502327.1:p.Ala278=
ENST00000675472.1:c.*242T>G	ENSP00000501946.1:n.*242T>G
ENST00000675474.1:n.341T>G
ENST00000675560.1:c.*366+993T>G	ENSP00000502118.1:n.*366+993T>G
ENST00000675625.1:c.*428T>G	ENSP00000501626.1:n.*428T>G
ENST00000675633.1:c.*163T>G	ENSP00000501785.1:n.*163T>G
ENST00000675661.1:c.*516T>G	ENSP00000501958.1:n.*516T>G
ENST00000675706.1:n.2714T>G
ENST00000675821.1:c.429T>G	ENSP00000502198.1:p.Ala143=
ENST00000675832.1:c.*428T>G	ENSP00000502041.1:n.*428T>G
ENST00000675928.1:c.582T>G	ENSP00000501568.1:p.Ala194=
ENST00000675944.1:c.552T>G	ENSP00000502673.1:p.Ala184=
ENST00000675999.1:c.694+993T>G	ENSP00000502572.1:n.694+993T>G
ENST00000676049.1:c.*658T>G	ENSP00000501912.1:n.*658T>G
ENST00000676112.1:c.822T>G	ENSP00000502295.1:p.Ala274=
ENST00000676143.1:c.429T>G	ENSP00000502828.1:p.Ala143=
ENST00000676207.1:c.694+993T>G	ENSP00000502638.1:n.694+993T>G
ENST00000676377.1:c.429T>G	ENSP00000502756.1:p.Ala143=
ENST00000676415.1:c.*62T>G	ENSP00000502665.1:n.*62T>G
ENST00000676443.1:c.708T>G	ENSP00000501769.1:p.Ala236=
ENST00000220822.11:c.756T>G	ENSP00000220822.7:p.Ala252=
ENST00000434412.2:c.552T>G	ENSP00000417006.2:p.Ala184=
ENST00000520797.5:n.521T>G
ENST00000521096.5:n.562T>G
ENST00000522568.1:c.*428T>G	ENSP00000430136.1:n.*428T>G
ENST00000524195.1:n.103+993T>G
NM_001040875.2:c.552T>G	NP_001035808.1:p.Ala184=
NM_018972.2:c.756T>G	NP_061845.2:p.Ala252=
NR_046346.1:n.690T>G
XM_011517551.1:c.1050T>G	XP_011515853.1:p.Ala350=
XM_011517552.1:c.429T>G	XP_011515854.1:p.Ala143=
NM_001040875.3:c.552T>G	NP_001035808.1:p.Ala184=
NM_001362929.1:c.429T>G	NP_001349858.1:p.Ala143=
NM_001362930.1:c.582T>G	NP_001349859.1:p.Ala194=
NM_001362931.1:c.694+993T>G	NP_001349860.1:n.694+993T>G
NM_001362932.1:c.429T>G	NP_001349861.1:p.Ala143=
NM_018972.3:c.756T>G	NP_061845.2:p.Ala252=
NM_001362931.2:c.694+993T>G	NP_001349860.1:n.694+993T>G
NM_018972.4:c.756T>G MANE Select	NP_061845.2:p.Ala252=
NM_001040875.4:c.552T>G	NP_001035808.1:p.Ala184=
NM_001362929.2:c.429T>G	NP_001349858.1:p.Ala143=
NM_001362930.2:c.582T>G	NP_001349859.1:p.Ala194=
NM_001362932.2:c.429T>G	NP_001349861.1:p.Ala143=