Canonical Allele Identifier: CA371550397

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276379A>C (hg19) ; chr8:g.74364144A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364144A>C , CM000670.2:g.74364144A>C	GRCh38
NC_000008.10:g.75276379A>C , CM000670.1:g.75276379A>C	GRCh37
NC_000008.9:g.75438934A>C	NCBI36
NG_008787.2:g.48015A>C
NG_008787.3:g.48015A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220822.12:c.854A>C MANE Select	ENSP00000220822.7:p.Lys285Thr
ENST00000434412.3:c.722A>C	ENSP00000417006.3:p.Lys241Thr
ENST00000520797.6:n.965A>C
ENST00000521096.6:n.710A>C
ENST00000522568.2:c.*526A>C	ENSP00000430136.1:n.*526A>C
ENST00000523640.2:c.165+12823A>C	ENSP00000502017.1:n.165+12823A>C
ENST00000524195.2:c.280+1091A>C	ENSP00000502308.1:n.280+1091A>C
ENST00000674612.1:c.527A>C	ENSP00000501864.1:p.Lys176Thr
ENST00000674710.1:c.694+1091A>C	ENSP00000502762.1:n.694+1091A>C
ENST00000674754.1:c.*2417A>C	ENSP00000502063.1:n.*2417A>C
ENST00000674756.1:c.*366+1091A>C	ENSP00000501860.1:n.*366+1091A>C
ENST00000674806.1:c.527A>C	ENSP00000502637.1:p.Lys176Thr
ENST00000674865.1:c.650A>C	ENSP00000502437.1:p.Lys217Thr
ENST00000674926.1:c.*1486A>C	ENSP00000501799.1:n.*1486A>C
ENST00000674934.1:c.*542A>C	ENSP00000502187.1:n.*542A>C
ENST00000674944.1:c.*1457A>C	ENSP00000501858.1:n.*1457A>C
ENST00000674946.1:c.694+1091A>C	ENSP00000501569.1:n.694+1091A>C
ENST00000674973.1:c.548A>C	ENSP00000502447.1:p.Lys183Thr
ENST00000675007.1:c.*592A>C	ENSP00000502119.1:n.*592A>C
ENST00000675060.1:c.*519A>C	ENSP00000501616.1:n.*519A>C
ENST00000675165.1:c.851A>C	ENSP00000502612.1:p.Lys284Thr
ENST00000675220.1:c.527A>C	ENSP00000502588.1:p.Lys176Thr
ENST00000675265.1:c.*604A>C	ENSP00000501848.1:n.*604A>C
ENST00000675336.1:c.*340A>C	ENSP00000502120.1:n.*340A>C
ENST00000675376.1:c.527A>C	ENSP00000502838.1:p.Lys176Thr
ENST00000675463.1:c.932A>C	ENSP00000502327.1:p.Lys311Thr
ENST00000675472.1:c.*340A>C	ENSP00000501946.1:n.*340A>C
ENST00000675474.1:n.439A>C
ENST00000675560.1:c.*366+1091A>C	ENSP00000502118.1:n.*366+1091A>C
ENST00000675625.1:c.*526A>C	ENSP00000501626.1:n.*526A>C
ENST00000675633.1:c.*261A>C	ENSP00000501785.1:n.*261A>C
ENST00000675661.1:c.*614A>C	ENSP00000501958.1:n.*614A>C
ENST00000675706.1:n.2812A>C
ENST00000675821.1:c.527A>C	ENSP00000502198.1:p.Lys176Thr
ENST00000675832.1:c.*526A>C	ENSP00000502041.1:n.*526A>C
ENST00000675928.1:c.680A>C	ENSP00000501568.1:p.Lys227Thr
ENST00000675944.1:c.650A>C	ENSP00000502673.1:p.Lys217Thr
ENST00000675999.1:c.694+1091A>C	ENSP00000502572.1:n.694+1091A>C
ENST00000676049.1:c.*756A>C	ENSP00000501912.1:n.*756A>C
ENST00000676112.1:c.920A>C	ENSP00000502295.1:p.Lys307Thr
ENST00000676143.1:c.527A>C	ENSP00000502828.1:p.Lys176Thr
ENST00000676207.1:c.694+1091A>C	ENSP00000502638.1:n.694+1091A>C
ENST00000676377.1:c.527A>C	ENSP00000502756.1:p.Lys176Thr
ENST00000676415.1:c.*160A>C	ENSP00000502665.1:n.*160A>C
ENST00000676443.1:c.806A>C	ENSP00000501769.1:p.Lys269Thr
ENST00000220822.11:c.854A>C	ENSP00000220822.7:p.Lys285Thr
ENST00000434412.2:c.650A>C	ENSP00000417006.2:p.Lys217Thr
ENST00000520797.5:n.619A>C
ENST00000521096.5:n.660A>C
ENST00000522568.1:c.*526A>C	ENSP00000430136.1:n.*526A>C
ENST00000524195.1:n.103+1091A>C
NM_001040875.2:c.650A>C	NP_001035808.1:p.Lys217Thr
NM_018972.2:c.854A>C	NP_061845.2:p.Lys285Thr
NR_046346.1:n.788A>C
XM_011517551.1:c.1148A>C	XP_011515853.1:p.Lys383Thr
XM_011517552.1:c.527A>C	XP_011515854.1:p.Lys176Thr
NM_001040875.3:c.650A>C	NP_001035808.1:p.Lys217Thr
NM_001362929.1:c.527A>C	NP_001349858.1:p.Lys176Thr
NM_001362930.1:c.680A>C	NP_001349859.1:p.Lys227Thr
NM_001362931.1:c.694+1091A>C	NP_001349860.1:n.694+1091A>C
NM_001362932.1:c.527A>C	NP_001349861.1:p.Lys176Thr
NM_018972.3:c.854A>C	NP_061845.2:p.Lys285Thr
NM_001362931.2:c.694+1091A>C	NP_001349860.1:n.694+1091A>C
NM_018972.4:c.854A>C MANE Select	NP_061845.2:p.Lys285Thr
NM_001040875.4:c.650A>C	NP_001035808.1:p.Lys217Thr
NM_001362929.2:c.527A>C	NP_001349858.1:p.Lys176Thr
NM_001362930.2:c.680A>C	NP_001349859.1:p.Lys227Thr
NM_001362932.2:c.527A>C	NP_001349861.1:p.Lys176Thr