Canonical Allele Identifier: CA461772392

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276308G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364073G>A , CM000670.2:g.74364073G>A	GRCh38
NC_000008.10:g.75276308G>A , CM000670.1:g.75276308G>A	GRCh37
NC_000008.9:g.75438863G>A	NCBI36
NG_008787.2:g.47944G>A
NG_008787.3:g.47944G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220822.12:c.783G>A MANE Select	ENSP00000220822.7:p.Leu261=
ENST00000434412.3:c.651G>A	ENSP00000417006.3:p.Leu217=
ENST00000520797.6:n.894G>A
ENST00000521096.6:n.639G>A
ENST00000522568.2:c.*455G>A	ENSP00000430136.1:n.*455G>A
ENST00000523640.2:c.165+12752G>A	ENSP00000502017.1:n.165+12752G>A
ENST00000524195.2:c.280+1020G>A	ENSP00000502308.1:n.280+1020G>A
ENST00000674612.1:c.456G>A	ENSP00000501864.1:p.Leu152=
ENST00000674710.1:c.694+1020G>A	ENSP00000502762.1:n.694+1020G>A
ENST00000674754.1:c.*2346G>A	ENSP00000502063.1:n.*2346G>A
ENST00000674756.1:c.*366+1020G>A	ENSP00000501860.1:n.*366+1020G>A
ENST00000674806.1:c.456G>A	ENSP00000502637.1:p.Leu152=
ENST00000674865.1:c.579G>A	ENSP00000502437.1:p.Leu193=
ENST00000674926.1:c.*1415G>A	ENSP00000501799.1:n.*1415G>A
ENST00000674934.1:c.*471G>A	ENSP00000502187.1:n.*471G>A
ENST00000674944.1:c.*1386G>A	ENSP00000501858.1:n.*1386G>A
ENST00000674946.1:c.694+1020G>A	ENSP00000501569.1:n.694+1020G>A
ENST00000674973.1:c.477G>A	ENSP00000502447.1:p.Leu159=
ENST00000675007.1:c.*521G>A	ENSP00000502119.1:n.*521G>A
ENST00000675060.1:c.*448G>A	ENSP00000501616.1:n.*448G>A
ENST00000675165.1:c.780G>A	ENSP00000502612.1:p.Leu260=
ENST00000675220.1:c.456G>A	ENSP00000502588.1:p.Leu152=
ENST00000675265.1:c.*533G>A	ENSP00000501848.1:n.*533G>A
ENST00000675336.1:c.*269G>A	ENSP00000502120.1:n.*269G>A
ENST00000675376.1:c.456G>A	ENSP00000502838.1:p.Leu152=
ENST00000675463.1:c.861G>A	ENSP00000502327.1:p.Leu287=
ENST00000675472.1:c.*269G>A	ENSP00000501946.1:n.*269G>A
ENST00000675474.1:n.368G>A
ENST00000675560.1:c.*366+1020G>A	ENSP00000502118.1:n.*366+1020G>A
ENST00000675625.1:c.*455G>A	ENSP00000501626.1:n.*455G>A
ENST00000675633.1:c.*190G>A	ENSP00000501785.1:n.*190G>A
ENST00000675661.1:c.*543G>A	ENSP00000501958.1:n.*543G>A
ENST00000675706.1:n.2741G>A
ENST00000675821.1:c.456G>A	ENSP00000502198.1:p.Leu152=
ENST00000675832.1:c.*455G>A	ENSP00000502041.1:n.*455G>A
ENST00000675928.1:c.609G>A	ENSP00000501568.1:p.Leu203=
ENST00000675944.1:c.579G>A	ENSP00000502673.1:p.Leu193=
ENST00000675999.1:c.694+1020G>A	ENSP00000502572.1:n.694+1020G>A
ENST00000676049.1:c.*685G>A	ENSP00000501912.1:n.*685G>A
ENST00000676112.1:c.849G>A	ENSP00000502295.1:p.Leu283=
ENST00000676143.1:c.456G>A	ENSP00000502828.1:p.Leu152=
ENST00000676207.1:c.694+1020G>A	ENSP00000502638.1:n.694+1020G>A
ENST00000676377.1:c.456G>A	ENSP00000502756.1:p.Leu152=
ENST00000676415.1:c.*89G>A	ENSP00000502665.1:n.*89G>A
ENST00000676443.1:c.735G>A	ENSP00000501769.1:p.Leu245=
ENST00000220822.11:c.783G>A	ENSP00000220822.7:p.Leu261=
ENST00000434412.2:c.579G>A	ENSP00000417006.2:p.Leu193=
ENST00000520797.5:n.548G>A
ENST00000521096.5:n.589G>A
ENST00000522568.1:c.*455G>A	ENSP00000430136.1:n.*455G>A
ENST00000524195.1:n.103+1020G>A
NM_001040875.2:c.579G>A	NP_001035808.1:p.Leu193=
NM_018972.2:c.783G>A	NP_061845.2:p.Leu261=
NR_046346.1:n.717G>A
XM_011517551.1:c.1077G>A	XP_011515853.1:p.Leu359=
XM_011517552.1:c.456G>A	XP_011515854.1:p.Leu152=
NM_001040875.3:c.579G>A	NP_001035808.1:p.Leu193=
NM_001362929.1:c.456G>A	NP_001349858.1:p.Leu152=
NM_001362930.1:c.609G>A	NP_001349859.1:p.Leu203=
NM_001362931.1:c.694+1020G>A	NP_001349860.1:n.694+1020G>A
NM_001362932.1:c.456G>A	NP_001349861.1:p.Leu152=
NM_018972.3:c.783G>A	NP_061845.2:p.Leu261=
NM_001362931.2:c.694+1020G>A	NP_001349860.1:n.694+1020G>A
NM_018972.4:c.783G>A MANE Select	NP_061845.2:p.Leu261=
NM_001040875.4:c.579G>A	NP_001035808.1:p.Leu193=
NM_001362929.2:c.456G>A	NP_001349858.1:p.Leu152=
NM_001362930.2:c.609G>A	NP_001349859.1:p.Leu203=
NM_001362932.2:c.456G>A	NP_001349861.1:p.Leu152=