Canonical Allele Identifier: CA371549844

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276229A>T (hg19) ; chr8:g.74363994A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74363994A>T , CM000670.2:g.74363994A>T	GRCh38
NC_000008.10:g.75276229A>T , CM000670.1:g.75276229A>T	GRCh37
NC_000008.9:g.75438784A>T	NCBI36
NG_008787.2:g.47865A>T
NG_008787.3:g.47865A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000220822.12:c.704A>T MANE Select	ENSP00000220822.7:p.Gln235Leu
ENST00000434412.3:c.572A>T	ENSP00000417006.3:p.Gln191Leu
ENST00000520797.6:n.815A>T
ENST00000521096.6:n.560A>T
ENST00000522568.2:c.*376A>T	ENSP00000430136.1:n.*376A>T
ENST00000523640.2:c.165+12673A>T	ENSP00000502017.1:n.165+12673A>T
ENST00000524195.2:c.280+941A>T	ENSP00000502308.1:n.280+941A>T
ENST00000674612.1:c.377A>T	ENSP00000501864.1:p.Gln126Leu
ENST00000674710.1:c.694+941A>T	ENSP00000502762.1:n.694+941A>T
ENST00000674754.1:c.*2267A>T	ENSP00000502063.1:n.*2267A>T
ENST00000674756.1:c.*366+941A>T	ENSP00000501860.1:n.*366+941A>T
ENST00000674806.1:c.377A>T	ENSP00000502637.1:p.Gln126Leu
ENST00000674865.1:c.500A>T	ENSP00000502437.1:p.Gln167Leu
ENST00000674926.1:c.*1336A>T	ENSP00000501799.1:n.*1336A>T
ENST00000674934.1:c.*392A>T	ENSP00000502187.1:n.*392A>T
ENST00000674944.1:c.*1307A>T	ENSP00000501858.1:n.*1307A>T
ENST00000674946.1:c.694+941A>T	ENSP00000501569.1:n.694+941A>T
ENST00000674973.1:c.398A>T	ENSP00000502447.1:p.Gln133Leu
ENST00000675007.1:c.*442A>T	ENSP00000502119.1:n.*442A>T
ENST00000675060.1:c.*369A>T	ENSP00000501616.1:n.*369A>T
ENST00000675165.1:c.701A>T	ENSP00000502612.1:p.Gln234Leu
ENST00000675220.1:c.377A>T	ENSP00000502588.1:p.Gln126Leu
ENST00000675265.1:c.*454A>T	ENSP00000501848.1:n.*454A>T
ENST00000675336.1:c.*190A>T	ENSP00000502120.1:n.*190A>T
ENST00000675376.1:c.377A>T	ENSP00000502838.1:p.Gln126Leu
ENST00000675463.1:c.782A>T	ENSP00000502327.1:p.Gln261Leu
ENST00000675472.1:c.*190A>T	ENSP00000501946.1:n.*190A>T
ENST00000675474.1:n.289A>T
ENST00000675560.1:c.*366+941A>T	ENSP00000502118.1:n.*366+941A>T
ENST00000675625.1:c.*376A>T	ENSP00000501626.1:n.*376A>T
ENST00000675633.1:c.*111A>T	ENSP00000501785.1:n.*111A>T
ENST00000675661.1:c.*464A>T	ENSP00000501958.1:n.*464A>T
ENST00000675706.1:n.2662A>T
ENST00000675821.1:c.377A>T	ENSP00000502198.1:p.Gln126Leu
ENST00000675832.1:c.*376A>T	ENSP00000502041.1:n.*376A>T
ENST00000675928.1:c.530A>T	ENSP00000501568.1:p.Gln177Leu
ENST00000675944.1:c.500A>T	ENSP00000502673.1:p.Gln167Leu
ENST00000675999.1:c.694+941A>T	ENSP00000502572.1:n.694+941A>T
ENST00000676049.1:c.*606A>T	ENSP00000501912.1:n.*606A>T
ENST00000676112.1:c.770A>T	ENSP00000502295.1:p.Gln257Leu
ENST00000676143.1:c.377A>T	ENSP00000502828.1:p.Gln126Leu
ENST00000676207.1:c.694+941A>T	ENSP00000502638.1:n.694+941A>T
ENST00000676377.1:c.377A>T	ENSP00000502756.1:p.Gln126Leu
ENST00000676415.1:c.*10A>T	ENSP00000502665.1:n.*10A>T
ENST00000676443.1:c.656A>T	ENSP00000501769.1:p.Gln219Leu
ENST00000220822.11:c.704A>T	ENSP00000220822.7:p.Gln235Leu
ENST00000434412.2:c.500A>T	ENSP00000417006.2:p.Gln167Leu
ENST00000520797.5:n.469A>T
ENST00000521096.5:n.510A>T
ENST00000522568.1:c.*376A>T	ENSP00000430136.1:n.*376A>T
ENST00000524195.1:n.103+941A>T
ENST00000524366.5:n.548A>T
NM_001040875.2:c.500A>T	NP_001035808.1:p.Gln167Leu
NM_018972.2:c.704A>T	NP_061845.2:p.Gln235Leu
NR_046346.1:n.638A>T
XM_011517551.1:c.998A>T	XP_011515853.1:p.Gln333Leu
XM_011517552.1:c.377A>T	XP_011515854.1:p.Gln126Leu
NM_001040875.3:c.500A>T	NP_001035808.1:p.Gln167Leu
NM_001362929.1:c.377A>T	NP_001349858.1:p.Gln126Leu
NM_001362930.1:c.530A>T	NP_001349859.1:p.Gln177Leu
NM_001362931.1:c.694+941A>T	NP_001349860.1:n.694+941A>T
NM_001362932.1:c.377A>T	NP_001349861.1:p.Gln126Leu
NM_018972.3:c.704A>T	NP_061845.2:p.Gln235Leu
NM_001362931.2:c.694+941A>T	NP_001349860.1:n.694+941A>T
NM_018972.4:c.704A>T MANE Select	NP_061845.2:p.Gln235Leu
NM_001040875.4:c.500A>T	NP_001035808.1:p.Gln167Leu
NM_001362929.2:c.377A>T	NP_001349858.1:p.Gln126Leu
NM_001362930.2:c.530A>T	NP_001349859.1:p.Gln177Leu
NM_001362932.2:c.377A>T	NP_001349861.1:p.Gln126Leu