Canonical Allele Identifier: CA116681
Gene: GDAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4190
ClinVar RCV Id: RCV000004409
dbSNP Id: rs121908112

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74350553G>A , CM000670.2:g.74350553G>A GRCh38
NC_000008.10:g.75262788G>A , CM000670.1:g.75262788G>A GRCh37
NC_000008.9:g.75425343G>A NCBI36
NG_008787.2:g.34424G>A
NG_008787.3:g.34424G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000220822.12:c.92G>A MANE Select ENSP00000220822.7:p.Trp31Ter
ENST00000434412.3:c.92G>A ENSP00000417006.3:p.Trp31Ter
ENST00000521096.6:n.341-11331G>A
ENST00000522568.2:c.92G>A ENSP00000430136.1:p.Trp31Ter
ENST00000523640.2:c.92G>A ENSP00000502017.1:p.Trp31Ter
ENST00000524195.2:c.92G>A ENSP00000502308.1:p.Trp31Ter
ENST00000524366.6:n.128G>A
ENST00000674612.1:c.-17-9584G>A ENSP00000501864.1:n.-17-9584G>A
ENST00000674710.1:c.92G>A ENSP00000502762.1:p.Trp31Ter
ENST00000674754.1:c.92G>A ENSP00000502063.1:p.Trp31Ter
ENST00000674756.1:c.92G>A ENSP00000501860.1:p.Trp31Ter
ENST00000674806.1:c.-66+188G>A ENSP00000502637.1:n.-66+188G>A
ENST00000674865.1:c.-64+81G>A ENSP00000502437.1:n.-64+81G>A
ENST00000674926.1:c.92G>A ENSP00000501799.1:p.Trp31Ter
ENST00000674934.1:c.92G>A ENSP00000502187.1:p.Trp31Ter
ENST00000674944.1:c.92G>A ENSP00000501858.1:p.Trp31Ter
ENST00000674946.1:c.92G>A ENSP00000501569.1:p.Trp31Ter
ENST00000674973.1:c.92G>A ENSP00000502447.1:p.Trp31Ter
ENST00000675007.1:c.92G>A ENSP00000502119.1:p.Trp31Ter
ENST00000675060.1:c.92G>A ENSP00000501616.1:p.Trp31Ter
ENST00000675165.1:c.92G>A ENSP00000502612.1:p.Trp31Ter
ENST00000675220.1:c.-17-9584G>A ENSP00000502588.1:n.-17-9584G>A
ENST00000675265.1:c.92G>A ENSP00000501848.1:p.Trp31Ter
ENST00000675336.1:c.92G>A ENSP00000502120.1:p.Trp31Ter
ENST00000675376.1:c.-17-9584G>A ENSP00000502838.1:n.-17-9584G>A
ENST00000675463.1:c.92G>A ENSP00000502327.1:p.Trp31Ter
ENST00000675472.1:c.92G>A ENSP00000501946.1:p.Trp31Ter
ENST00000675560.1:c.92G>A ENSP00000502118.1:p.Trp31Ter
ENST00000675625.1:c.92G>A ENSP00000501626.1:p.Trp31Ter
ENST00000675633.1:c.92G>A ENSP00000501785.1:p.Trp31Ter
ENST00000675661.1:c.92G>A ENSP00000501958.1:p.Trp31Ter
ENST00000675706.1:n.159G>A
ENST00000675821.1:c.-17-9584G>A ENSP00000502198.1:n.-17-9584G>A
ENST00000675832.1:c.92G>A ENSP00000502041.1:p.Trp31Ter
ENST00000675928.1:c.92G>A ENSP00000501568.1:p.Trp31Ter
ENST00000675944.1:c.-88+188G>A ENSP00000502673.1:n.-88+188G>A
ENST00000675999.1:c.92G>A ENSP00000502572.1:p.Trp31Ter
ENST00000676049.1:c.92G>A ENSP00000501912.1:p.Trp31Ter
ENST00000676112.1:c.92G>A ENSP00000502295.1:p.Trp31Ter
ENST00000676120.1:c.92G>A ENSP00000502036.1:p.Trp31Ter
ENST00000676143.1:c.-17-9584G>A ENSP00000502828.1:n.-17-9584G>A
ENST00000676207.1:c.92G>A ENSP00000502638.1:p.Trp31Ter
ENST00000676377.1:c.-17-9584G>A ENSP00000502756.1:n.-17-9584G>A
ENST00000676415.1:c.92G>A ENSP00000502665.1:p.Trp31Ter
ENST00000676443.1:c.69+23G>A ENSP00000501769.1:n.69+23G>A
ENST00000220822.11:c.92G>A ENSP00000220822.7:p.Trp31Ter
ENST00000434412.2:c.-64+81G>A ENSP00000417006.2:n.-64+81G>A
ENST00000520797.5:n.76-9584G>A
ENST00000521096.5:n.117-9584G>A
ENST00000522568.1:c.92G>A ENSP00000430136.1:p.Trp31Ter
ENST00000523640.1:n.120G>A
ENST00000524366.5:n.110G>A
NM_001040875.2:c.-64+81G>A NP_001035808.1:n.-64+81G>A
NM_018972.2:c.92G>A NP_061845.2:p.Trp31Ter
NR_046346.1:n.171G>A
XM_011517551.1:c.560G>A XP_011515853.1:p.Trp187Ter
XM_011517552.1:c.-43G>A XP_011515854.1:n.-43G>A
NM_001040875.3:c.-64+81G>A NP_001035808.1:n.-64+81G>A
NM_001362929.1:c.-91G>A NP_001349858.1:n.-91G>A
NM_001362930.1:c.92G>A NP_001349859.1:p.Trp31Ter
NM_001362931.1:c.92G>A NP_001349860.1:p.Trp31Ter
NM_001362932.1:c.-43G>A NP_001349861.1:n.-43G>A
NM_018972.3:c.92G>A NP_061845.2:p.Trp31Ter
XM_017013586.2:c.92G>A XP_016869075.2:p.Trp31Ter
NM_001362931.2:c.92G>A NP_001349860.1:p.Trp31Ter
NM_018972.4:c.92G>A MANE Select NP_061845.2:p.Trp31Ter
NM_001040875.4:c.-64+81G>A NP_001035808.1:n.-64+81G>A
NM_001362929.2:c.-91G>A NP_001349858.1:n.-91G>A
NM_001362930.2:c.92G>A NP_001349859.1:p.Trp31Ter
NM_001362932.2:c.-43G>A NP_001349861.1:n.-43G>A