Canonical Allele Identifier: CA371550673

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276509G>C (hg19) ; chr8:g.74364274G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364274G>C , CM000670.2:g.74364274G>C	GRCh38
NC_000008.10:g.75276509G>C , CM000670.1:g.75276509G>C	GRCh37
NC_000008.9:g.75439064G>C	NCBI36
NG_008787.2:g.48145G>C
NG_008787.3:g.48145G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000220822.12:c.984G>C MANE Select	ENSP00000220822.7:p.Leu328Phe
ENST00000434412.3:c.852G>C	ENSP00000417006.3:p.Leu284Phe
ENST00000520797.6:n.1095G>C
ENST00000521096.6:n.840G>C
ENST00000522568.2:c.*545+111G>C	ENSP00000430136.1:n.*545+111G>C
ENST00000523640.2:c.165+12953G>C	ENSP00000502017.1:n.165+12953G>C
ENST00000524195.2:c.280+1221G>C	ENSP00000502308.1:n.280+1221G>C
ENST00000674612.1:c.657G>C	ENSP00000501864.1:p.Leu219Phe
ENST00000674710.1:c.694+1221G>C	ENSP00000502762.1:n.694+1221G>C
ENST00000674754.1:c.*2547G>C	ENSP00000502063.1:n.*2547G>C
ENST00000674756.1:c.*366+1221G>C	ENSP00000501860.1:n.*366+1221G>C
ENST00000674806.1:c.657G>C	ENSP00000502637.1:p.Leu219Phe
ENST00000674865.1:c.780G>C	ENSP00000502437.1:p.Leu260Phe
ENST00000674926.1:c.*1616G>C	ENSP00000501799.1:n.*1616G>C
ENST00000674934.1:c.*672G>C	ENSP00000502187.1:n.*672G>C
ENST00000674944.1:c.*1587G>C	ENSP00000501858.1:n.*1587G>C
ENST00000674946.1:c.694+1221G>C	ENSP00000501569.1:n.694+1221G>C
ENST00000674973.1:c.678G>C	ENSP00000502447.1:p.Leu226Phe
ENST00000675007.1:c.*722G>C	ENSP00000502119.1:n.*722G>C
ENST00000675060.1:c.*649G>C	ENSP00000501616.1:n.*649G>C
ENST00000675165.1:c.981G>C	ENSP00000502612.1:p.Leu327Phe
ENST00000675220.1:c.657G>C	ENSP00000502588.1:p.Leu219Phe
ENST00000675265.1:c.*734G>C	ENSP00000501848.1:n.*734G>C
ENST00000675336.1:c.*470G>C	ENSP00000502120.1:n.*470G>C
ENST00000675376.1:c.657G>C	ENSP00000502838.1:p.Leu219Phe
ENST00000675463.1:c.1062G>C	ENSP00000502327.1:p.Leu354Phe
ENST00000675472.1:c.*470G>C	ENSP00000501946.1:n.*470G>C
ENST00000675474.1:n.569G>C
ENST00000675560.1:c.*366+1221G>C	ENSP00000502118.1:n.*366+1221G>C
ENST00000675625.1:c.*656G>C	ENSP00000501626.1:n.*656G>C
ENST00000675633.1:c.*391G>C	ENSP00000501785.1:n.*391G>C
ENST00000675661.1:c.*744G>C	ENSP00000501958.1:n.*744G>C
ENST00000675706.1:n.2942G>C
ENST00000675821.1:c.657G>C	ENSP00000502198.1:p.Leu219Phe
ENST00000675832.1:c.*656G>C	ENSP00000502041.1:n.*656G>C
ENST00000675928.1:c.810G>C	ENSP00000501568.1:p.Leu270Phe
ENST00000675944.1:c.780G>C	ENSP00000502673.1:p.Leu260Phe
ENST00000675999.1:c.694+1221G>C	ENSP00000502572.1:n.694+1221G>C
ENST00000676049.1:c.*886G>C	ENSP00000501912.1:n.*886G>C
ENST00000676112.1:c.1050G>C	ENSP00000502295.1:p.Leu350Phe
ENST00000676143.1:c.657G>C	ENSP00000502828.1:p.Leu219Phe
ENST00000676207.1:c.694+1221G>C	ENSP00000502638.1:n.694+1221G>C
ENST00000676377.1:c.657G>C	ENSP00000502756.1:p.Leu219Phe
ENST00000676415.1:c.*290G>C	ENSP00000502665.1:n.*290G>C
ENST00000676443.1:c.936G>C	ENSP00000501769.1:p.Leu312Phe
ENST00000220822.11:c.984G>C	ENSP00000220822.7:p.Leu328Phe
ENST00000434412.2:c.780G>C	ENSP00000417006.2:p.Leu260Phe
ENST00000521096.5:n.790G>C
ENST00000522568.1:c.*656G>C	ENSP00000430136.1:n.*656G>C
ENST00000524195.1:n.103+1221G>C
NM_001040875.2:c.780G>C	NP_001035808.1:p.Leu260Phe
NM_018972.2:c.984G>C	NP_061845.2:p.Leu328Phe
NR_046346.1:n.918G>C
XM_011517551.1:c.1278G>C	XP_011515853.1:p.Leu426Phe
XM_011517552.1:c.657G>C	XP_011515854.1:p.Leu219Phe
NM_001040875.3:c.780G>C	NP_001035808.1:p.Leu260Phe
NM_001362929.1:c.657G>C	NP_001349858.1:p.Leu219Phe
NM_001362930.1:c.810G>C	NP_001349859.1:p.Leu270Phe
NM_001362931.1:c.694+1221G>C	NP_001349860.1:n.694+1221G>C
NM_001362932.1:c.657G>C	NP_001349861.1:p.Leu219Phe
NM_018972.3:c.984G>C	NP_061845.2:p.Leu328Phe
NM_001362931.2:c.694+1221G>C	NP_001349860.1:n.694+1221G>C
NM_018972.4:c.984G>C MANE Select	NP_061845.2:p.Leu328Phe
NM_001040875.4:c.780G>C	NP_001035808.1:p.Leu260Phe
NM_001362929.2:c.657G>C	NP_001349858.1:p.Leu219Phe
NM_001362930.2:c.810G>C	NP_001349859.1:p.Leu270Phe
NM_001362932.2:c.657G>C	NP_001349861.1:p.Leu219Phe