Canonical Allele Identifier: CA371550687

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276516G>C (hg19) ; chr8:g.74364281G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364281G>C , CM000670.2:g.74364281G>C	GRCh38
NC_000008.10:g.75276516G>C , CM000670.1:g.75276516G>C	GRCh37
NC_000008.9:g.75439071G>C	NCBI36
NG_008787.2:g.48152G>C
NG_008787.3:g.48152G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000220822.12:c.991G>C MANE Select	ENSP00000220822.7:p.Gly331Arg
ENST00000434412.3:c.859G>C	ENSP00000417006.3:p.Gly287Arg
ENST00000520797.6:n.1102G>C
ENST00000521096.6:n.847G>C
ENST00000522568.2:c.*545+118G>C	ENSP00000430136.1:n.*545+118G>C
ENST00000523640.2:c.165+12960G>C	ENSP00000502017.1:n.165+12960G>C
ENST00000524195.2:c.280+1228G>C	ENSP00000502308.1:n.280+1228G>C
ENST00000674612.1:c.664G>C	ENSP00000501864.1:p.Gly222Arg
ENST00000674710.1:c.694+1228G>C	ENSP00000502762.1:n.694+1228G>C
ENST00000674754.1:c.*2554G>C	ENSP00000502063.1:n.*2554G>C
ENST00000674756.1:c.*366+1228G>C	ENSP00000501860.1:n.*366+1228G>C
ENST00000674806.1:c.664G>C	ENSP00000502637.1:p.Gly222Arg
ENST00000674865.1:c.787G>C	ENSP00000502437.1:p.Gly263Arg
ENST00000674926.1:c.*1623G>C	ENSP00000501799.1:n.*1623G>C
ENST00000674934.1:c.*679G>C	ENSP00000502187.1:n.*679G>C
ENST00000674944.1:c.*1594G>C	ENSP00000501858.1:n.*1594G>C
ENST00000674946.1:c.694+1228G>C	ENSP00000501569.1:n.694+1228G>C
ENST00000674973.1:c.685G>C	ENSP00000502447.1:p.Gly229Arg
ENST00000675007.1:c.*729G>C	ENSP00000502119.1:n.*729G>C
ENST00000675060.1:c.*656G>C	ENSP00000501616.1:n.*656G>C
ENST00000675165.1:c.988G>C	ENSP00000502612.1:p.Gly330Arg
ENST00000675220.1:c.664G>C	ENSP00000502588.1:p.Gly222Arg
ENST00000675265.1:c.*741G>C	ENSP00000501848.1:n.*741G>C
ENST00000675336.1:c.*477G>C	ENSP00000502120.1:n.*477G>C
ENST00000675376.1:c.664G>C	ENSP00000502838.1:p.Gly222Arg
ENST00000675463.1:c.1069G>C	ENSP00000502327.1:p.Gly357Arg
ENST00000675472.1:c.*477G>C	ENSP00000501946.1:n.*477G>C
ENST00000675474.1:n.576G>C
ENST00000675560.1:c.*366+1228G>C	ENSP00000502118.1:n.*366+1228G>C
ENST00000675625.1:c.*663G>C	ENSP00000501626.1:n.*663G>C
ENST00000675633.1:c.*398G>C	ENSP00000501785.1:n.*398G>C
ENST00000675661.1:c.*751G>C	ENSP00000501958.1:n.*751G>C
ENST00000675706.1:n.2949G>C
ENST00000675821.1:c.664G>C	ENSP00000502198.1:p.Gly222Arg
ENST00000675832.1:c.*663G>C	ENSP00000502041.1:n.*663G>C
ENST00000675928.1:c.817G>C	ENSP00000501568.1:p.Gly273Arg
ENST00000675944.1:c.787G>C	ENSP00000502673.1:p.Gly263Arg
ENST00000675999.1:c.694+1228G>C	ENSP00000502572.1:n.694+1228G>C
ENST00000676049.1:c.*893G>C	ENSP00000501912.1:n.*893G>C
ENST00000676112.1:c.1057G>C	ENSP00000502295.1:p.Gly353Arg
ENST00000676143.1:c.664G>C	ENSP00000502828.1:p.Gly222Arg
ENST00000676207.1:c.694+1228G>C	ENSP00000502638.1:n.694+1228G>C
ENST00000676377.1:c.664G>C	ENSP00000502756.1:p.Gly222Arg
ENST00000676415.1:c.*297G>C	ENSP00000502665.1:n.*297G>C
ENST00000676443.1:c.943G>C	ENSP00000501769.1:p.Gly315Arg
ENST00000220822.11:c.991G>C	ENSP00000220822.7:p.Gly331Arg
ENST00000434412.2:c.787G>C	ENSP00000417006.2:p.Gly263Arg
ENST00000521096.5:n.797G>C
ENST00000522568.1:c.*663G>C	ENSP00000430136.1:n.*663G>C
ENST00000524195.1:n.103+1228G>C
NM_001040875.2:c.787G>C	NP_001035808.1:p.Gly263Arg
NM_018972.2:c.991G>C	NP_061845.2:p.Gly331Arg
NR_046346.1:n.925G>C
XM_011517551.1:c.1285G>C	XP_011515853.1:p.Gly429Arg
XM_011517552.1:c.664G>C	XP_011515854.1:p.Gly222Arg
NM_001040875.3:c.787G>C	NP_001035808.1:p.Gly263Arg
NM_001362929.1:c.664G>C	NP_001349858.1:p.Gly222Arg
NM_001362930.1:c.817G>C	NP_001349859.1:p.Gly273Arg
NM_001362931.1:c.694+1228G>C	NP_001349860.1:n.694+1228G>C
NM_001362932.1:c.664G>C	NP_001349861.1:p.Gly222Arg
NM_018972.3:c.991G>C	NP_061845.2:p.Gly331Arg
NM_001362931.2:c.694+1228G>C	NP_001349860.1:n.694+1228G>C
NM_018972.4:c.991G>C MANE Select	NP_061845.2:p.Gly331Arg
NM_001040875.4:c.787G>C	NP_001035808.1:p.Gly263Arg
NM_001362929.2:c.664G>C	NP_001349858.1:p.Gly222Arg
NM_001362930.2:c.817G>C	NP_001349859.1:p.Gly273Arg
NM_001362932.2:c.664G>C	NP_001349861.1:p.Gly222Arg