Canonical Allele Identifier: CA371549886

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276238G>C (hg19) ; chr8:g.74364003G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364003G>C , CM000670.2:g.74364003G>C	GRCh38
NC_000008.10:g.75276238G>C , CM000670.1:g.75276238G>C	GRCh37
NC_000008.9:g.75438793G>C	NCBI36
NG_008787.2:g.47874G>C
NG_008787.3:g.47874G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220822.12:c.713G>C MANE Select	ENSP00000220822.7:p.Trp238Ser
ENST00000434412.3:c.581G>C	ENSP00000417006.3:p.Trp194Ser
ENST00000520797.6:n.824G>C
ENST00000521096.6:n.569G>C
ENST00000522568.2:c.*385G>C	ENSP00000430136.1:n.*385G>C
ENST00000523640.2:c.165+12682G>C	ENSP00000502017.1:n.165+12682G>C
ENST00000524195.2:c.280+950G>C	ENSP00000502308.1:n.280+950G>C
ENST00000674612.1:c.386G>C	ENSP00000501864.1:p.Trp129Ser
ENST00000674710.1:c.694+950G>C	ENSP00000502762.1:n.694+950G>C
ENST00000674754.1:c.*2276G>C	ENSP00000502063.1:n.*2276G>C
ENST00000674756.1:c.*366+950G>C	ENSP00000501860.1:n.*366+950G>C
ENST00000674806.1:c.386G>C	ENSP00000502637.1:p.Trp129Ser
ENST00000674865.1:c.509G>C	ENSP00000502437.1:p.Trp170Ser
ENST00000674926.1:c.*1345G>C	ENSP00000501799.1:n.*1345G>C
ENST00000674934.1:c.*401G>C	ENSP00000502187.1:n.*401G>C
ENST00000674944.1:c.*1316G>C	ENSP00000501858.1:n.*1316G>C
ENST00000674946.1:c.694+950G>C	ENSP00000501569.1:n.694+950G>C
ENST00000674973.1:c.407G>C	ENSP00000502447.1:p.Trp136Ser
ENST00000675007.1:c.*451G>C	ENSP00000502119.1:n.*451G>C
ENST00000675060.1:c.*378G>C	ENSP00000501616.1:n.*378G>C
ENST00000675165.1:c.710G>C	ENSP00000502612.1:p.Trp237Ser
ENST00000675220.1:c.386G>C	ENSP00000502588.1:p.Trp129Ser
ENST00000675265.1:c.*463G>C	ENSP00000501848.1:n.*463G>C
ENST00000675336.1:c.*199G>C	ENSP00000502120.1:n.*199G>C
ENST00000675376.1:c.386G>C	ENSP00000502838.1:p.Trp129Ser
ENST00000675463.1:c.791G>C	ENSP00000502327.1:p.Trp264Ser
ENST00000675472.1:c.*199G>C	ENSP00000501946.1:n.*199G>C
ENST00000675474.1:n.298G>C
ENST00000675560.1:c.*366+950G>C	ENSP00000502118.1:n.*366+950G>C
ENST00000675625.1:c.*385G>C	ENSP00000501626.1:n.*385G>C
ENST00000675633.1:c.*120G>C	ENSP00000501785.1:n.*120G>C
ENST00000675661.1:c.*473G>C	ENSP00000501958.1:n.*473G>C
ENST00000675706.1:n.2671G>C
ENST00000675821.1:c.386G>C	ENSP00000502198.1:p.Trp129Ser
ENST00000675832.1:c.*385G>C	ENSP00000502041.1:n.*385G>C
ENST00000675928.1:c.539G>C	ENSP00000501568.1:p.Trp180Ser
ENST00000675944.1:c.509G>C	ENSP00000502673.1:p.Trp170Ser
ENST00000675999.1:c.694+950G>C	ENSP00000502572.1:n.694+950G>C
ENST00000676049.1:c.*615G>C	ENSP00000501912.1:n.*615G>C
ENST00000676112.1:c.779G>C	ENSP00000502295.1:p.Trp260Ser
ENST00000676143.1:c.386G>C	ENSP00000502828.1:p.Trp129Ser
ENST00000676207.1:c.694+950G>C	ENSP00000502638.1:n.694+950G>C
ENST00000676377.1:c.386G>C	ENSP00000502756.1:p.Trp129Ser
ENST00000676415.1:c.*19G>C	ENSP00000502665.1:n.*19G>C
ENST00000676443.1:c.665G>C	ENSP00000501769.1:p.Trp222Ser
ENST00000220822.11:c.713G>C	ENSP00000220822.7:p.Trp238Ser
ENST00000434412.2:c.509G>C	ENSP00000417006.2:p.Trp170Ser
ENST00000520797.5:n.478G>C
ENST00000521096.5:n.519G>C
ENST00000522568.1:c.*385G>C	ENSP00000430136.1:n.*385G>C
ENST00000524195.1:n.103+950G>C
ENST00000524366.5:n.557G>C
NM_001040875.2:c.509G>C	NP_001035808.1:p.Trp170Ser
NM_018972.2:c.713G>C	NP_061845.2:p.Trp238Ser
NR_046346.1:n.647G>C
XM_011517551.1:c.1007G>C	XP_011515853.1:p.Trp336Ser
XM_011517552.1:c.386G>C	XP_011515854.1:p.Trp129Ser
NM_001040875.3:c.509G>C	NP_001035808.1:p.Trp170Ser
NM_001362929.1:c.386G>C	NP_001349858.1:p.Trp129Ser
NM_001362930.1:c.539G>C	NP_001349859.1:p.Trp180Ser
NM_001362931.1:c.694+950G>C	NP_001349860.1:n.694+950G>C
NM_001362932.1:c.386G>C	NP_001349861.1:p.Trp129Ser
NM_018972.3:c.713G>C	NP_061845.2:p.Trp238Ser
NM_001362931.2:c.694+950G>C	NP_001349860.1:n.694+950G>C
NM_018972.4:c.713G>C MANE Select	NP_061845.2:p.Trp238Ser
NM_001040875.4:c.509G>C	NP_001035808.1:p.Trp170Ser
NM_001362929.2:c.386G>C	NP_001349858.1:p.Trp129Ser
NM_001362930.2:c.539G>C	NP_001349859.1:p.Trp180Ser
NM_001362932.2:c.386G>C	NP_001349861.1:p.Trp129Ser