Canonical Allele Identifier: CA1794115953

Gene: GDAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74363756G= , CM000670.2:g.74363756G=	GRCh38
NC_000008.10:g.75275991G= , CM000670.1:g.75275991G=	GRCh37
NC_000008.9:g.75438546G=	NCBI36
NG_008787.2:g.47627G=
NG_008787.3:g.47627G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220822.12:c.695-229G= MANE Select	ENSP00000220822.7:n.695-229G=
ENST00000434412.3:c.563-229G=	ENSP00000417006.3:n.563-229G=
ENST00000520797.6:n.806-229G=
ENST00000521096.6:n.551-229G=
ENST00000522568.2:c.*367-229G=	ENSP00000430136.1:n.*367-229G=
ENST00000523640.2:c.165+12435G=	ENSP00000502017.1:n.165+12435G=
ENST00000524195.2:c.280+703G=	ENSP00000502308.1:n.280+703G=
ENST00000674612.1:c.368-229G=	ENSP00000501864.1:n.368-229G=
ENST00000674710.1:c.694+703G=	ENSP00000502762.1:n.694+703G=
ENST00000674754.1:c.*2029G=	ENSP00000502063.1:n.*2029G=
ENST00000674756.1:c.*366+703G=	ENSP00000501860.1:n.*366+703G=
ENST00000674806.1:c.368-229G=	ENSP00000502637.1:n.368-229G=
ENST00000674865.1:c.491-229G=	ENSP00000502437.1:n.491-229G=
ENST00000674926.1:c.*1327-229G=	ENSP00000501799.1:n.*1327-229G=
ENST00000674934.1:c.*383-229G=	ENSP00000502187.1:n.*383-229G=
ENST00000674944.1:c.*1069G=	ENSP00000501858.1:n.*1069G=
ENST00000674946.1:c.694+703G=	ENSP00000501569.1:n.694+703G=
ENST00000674973.1:c.389-229G=	ENSP00000502447.1:n.389-229G=
ENST00000675007.1:c.*433-229G=	ENSP00000502119.1:n.*433-229G=
ENST00000675060.1:c.*360-229G=	ENSP00000501616.1:n.*360-229G=
ENST00000675165.1:c.695-232G=	ENSP00000502612.1:n.695-232G=
ENST00000675220.1:c.368-229G=	ENSP00000502588.1:n.368-229G=
ENST00000675265.1:c.*445-229G=	ENSP00000501848.1:n.*445-229G=
ENST00000675336.1:c.*181-229G=	ENSP00000502120.1:n.*181-229G=
ENST00000675376.1:c.368-229G=	ENSP00000502838.1:n.368-229G=
ENST00000675463.1:c.773-229G=	ENSP00000502327.1:n.773-229G=
ENST00000675472.1:c.*181-229G=	ENSP00000501946.1:n.*181-229G=
ENST00000675474.1:n.280-229G=
ENST00000675560.1:c.*366+703G=	ENSP00000502118.1:n.*366+703G=
ENST00000675625.1:c.*367-229G=	ENSP00000501626.1:n.*367-229G=
ENST00000675633.1:c.*102-229G=	ENSP00000501785.1:n.*102-229G=
ENST00000675661.1:c.*455-229G=	ENSP00000501958.1:n.*455-229G=
ENST00000675706.1:n.2424G=
ENST00000675821.1:c.368-229G=	ENSP00000502198.1:n.368-229G=
ENST00000675832.1:c.*367-229G=	ENSP00000502041.1:n.*367-229G=
ENST00000675928.1:c.521-229G=	ENSP00000501568.1:n.521-229G=
ENST00000675944.1:c.491-229G=	ENSP00000502673.1:n.491-229G=
ENST00000675999.1:c.694+703G=	ENSP00000502572.1:n.694+703G=
ENST00000676049.1:c.*597-229G=	ENSP00000501912.1:n.*597-229G=
ENST00000676112.1:c.761-229G=	ENSP00000502295.1:n.761-229G=
ENST00000676143.1:c.368-229G=	ENSP00000502828.1:n.368-229G=
ENST00000676207.1:c.694+703G=	ENSP00000502638.1:n.694+703G=
ENST00000676377.1:c.368-229G=	ENSP00000502756.1:n.368-229G=
ENST00000676415.1:c.695-188G=	ENSP00000502665.1:n.695-188G=
ENST00000676443.1:c.647-229G=	ENSP00000501769.1:n.647-229G=
ENST00000220822.11:c.695-229G=	ENSP00000220822.7:n.695-229G=
ENST00000434412.2:c.491-229G=	ENSP00000417006.2:n.491-229G=
ENST00000520797.5:n.460-229G=
ENST00000521096.5:n.501-229G=
ENST00000522568.1:c.*367-229G=	ENSP00000430136.1:n.*367-229G=
ENST00000524195.1:n.103+703G=
ENST00000524366.5:n.539-229G=
NM_001040875.2:c.491-229G=	NP_001035808.1:n.491-229G=
NM_018972.2:c.695-229G=	NP_061845.2:n.695-229G=
NR_046346.1:n.629-229G=
XM_011517551.1:c.989-229G=	XP_011515853.1:n.989-229G=
XM_011517552.1:c.368-229G=	XP_011515854.1:n.368-229G=
NM_001040875.3:c.491-229G=	NP_001035808.1:n.491-229G=
NM_001362929.1:c.368-229G=	NP_001349858.1:n.368-229G=
NM_001362930.1:c.521-229G=	NP_001349859.1:n.521-229G=
NM_001362931.1:c.694+703G=	NP_001349860.1:n.694+703G=
NM_001362932.1:c.368-229G=	NP_001349861.1:n.368-229G=
NM_018972.3:c.695-229G=	NP_061845.2:n.695-229G=
NM_001362931.2:c.694+703G=	NP_001349860.1:n.694+703G=
NM_018972.4:c.695-229G= MANE Select	NP_061845.2:n.695-229G=
NM_001040875.4:c.491-229G=	NP_001035808.1:n.491-229G=
NM_001362929.2:c.368-229G=	NP_001349858.1:n.368-229G=
NM_001362930.2:c.521-229G=	NP_001349859.1:n.521-229G=
NM_001362932.2:c.368-229G=	NP_001349861.1:n.368-229G=