Canonical Allele Identifier: CA371550238

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276315G>A (hg19) ; chr8:g.74364080G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364080G>A , CM000670.2:g.74364080G>A	GRCh38
NC_000008.10:g.75276315G>A , CM000670.1:g.75276315G>A	GRCh37
NC_000008.9:g.75438870G>A	NCBI36
NG_008787.2:g.47951G>A
NG_008787.3:g.47951G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220822.12:c.790G>A MANE Select	ENSP00000220822.7:p.Ala264Thr
ENST00000434412.3:c.658G>A	ENSP00000417006.3:p.Ala220Thr
ENST00000520797.6:n.901G>A
ENST00000521096.6:n.646G>A
ENST00000522568.2:c.*462G>A	ENSP00000430136.1:n.*462G>A
ENST00000523640.2:c.165+12759G>A	ENSP00000502017.1:n.165+12759G>A
ENST00000524195.2:c.280+1027G>A	ENSP00000502308.1:n.280+1027G>A
ENST00000674612.1:c.463G>A	ENSP00000501864.1:p.Ala155Thr
ENST00000674710.1:c.694+1027G>A	ENSP00000502762.1:n.694+1027G>A
ENST00000674754.1:c.*2353G>A	ENSP00000502063.1:n.*2353G>A
ENST00000674756.1:c.*366+1027G>A	ENSP00000501860.1:n.*366+1027G>A
ENST00000674806.1:c.463G>A	ENSP00000502637.1:p.Ala155Thr
ENST00000674865.1:c.586G>A	ENSP00000502437.1:p.Ala196Thr
ENST00000674926.1:c.*1422G>A	ENSP00000501799.1:n.*1422G>A
ENST00000674934.1:c.*478G>A	ENSP00000502187.1:n.*478G>A
ENST00000674944.1:c.*1393G>A	ENSP00000501858.1:n.*1393G>A
ENST00000674946.1:c.694+1027G>A	ENSP00000501569.1:n.694+1027G>A
ENST00000674973.1:c.484G>A	ENSP00000502447.1:p.Ala162Thr
ENST00000675007.1:c.*528G>A	ENSP00000502119.1:n.*528G>A
ENST00000675060.1:c.*455G>A	ENSP00000501616.1:n.*455G>A
ENST00000675165.1:c.787G>A	ENSP00000502612.1:p.Ala263Thr
ENST00000675220.1:c.463G>A	ENSP00000502588.1:p.Ala155Thr
ENST00000675265.1:c.*540G>A	ENSP00000501848.1:n.*540G>A
ENST00000675336.1:c.*276G>A	ENSP00000502120.1:n.*276G>A
ENST00000675376.1:c.463G>A	ENSP00000502838.1:p.Ala155Thr
ENST00000675463.1:c.868G>A	ENSP00000502327.1:p.Ala290Thr
ENST00000675472.1:c.*276G>A	ENSP00000501946.1:n.*276G>A
ENST00000675474.1:n.375G>A
ENST00000675560.1:c.*366+1027G>A	ENSP00000502118.1:n.*366+1027G>A
ENST00000675625.1:c.*462G>A	ENSP00000501626.1:n.*462G>A
ENST00000675633.1:c.*197G>A	ENSP00000501785.1:n.*197G>A
ENST00000675661.1:c.*550G>A	ENSP00000501958.1:n.*550G>A
ENST00000675706.1:n.2748G>A
ENST00000675821.1:c.463G>A	ENSP00000502198.1:p.Ala155Thr
ENST00000675832.1:c.*462G>A	ENSP00000502041.1:n.*462G>A
ENST00000675928.1:c.616G>A	ENSP00000501568.1:p.Ala206Thr
ENST00000675944.1:c.586G>A	ENSP00000502673.1:p.Ala196Thr
ENST00000675999.1:c.694+1027G>A	ENSP00000502572.1:n.694+1027G>A
ENST00000676049.1:c.*692G>A	ENSP00000501912.1:n.*692G>A
ENST00000676112.1:c.856G>A	ENSP00000502295.1:p.Ala286Thr
ENST00000676143.1:c.463G>A	ENSP00000502828.1:p.Ala155Thr
ENST00000676207.1:c.694+1027G>A	ENSP00000502638.1:n.694+1027G>A
ENST00000676377.1:c.463G>A	ENSP00000502756.1:p.Ala155Thr
ENST00000676415.1:c.*96G>A	ENSP00000502665.1:n.*96G>A
ENST00000676443.1:c.742G>A	ENSP00000501769.1:p.Ala248Thr
ENST00000220822.11:c.790G>A	ENSP00000220822.7:p.Ala264Thr
ENST00000434412.2:c.586G>A	ENSP00000417006.2:p.Ala196Thr
ENST00000520797.5:n.555G>A
ENST00000521096.5:n.596G>A
ENST00000522568.1:c.*462G>A	ENSP00000430136.1:n.*462G>A
ENST00000524195.1:n.103+1027G>A
NM_001040875.2:c.586G>A	NP_001035808.1:p.Ala196Thr
NM_018972.2:c.790G>A	NP_061845.2:p.Ala264Thr
NR_046346.1:n.724G>A
XM_011517551.1:c.1084G>A	XP_011515853.1:p.Ala362Thr
XM_011517552.1:c.463G>A	XP_011515854.1:p.Ala155Thr
NM_001040875.3:c.586G>A	NP_001035808.1:p.Ala196Thr
NM_001362929.1:c.463G>A	NP_001349858.1:p.Ala155Thr
NM_001362930.1:c.616G>A	NP_001349859.1:p.Ala206Thr
NM_001362931.1:c.694+1027G>A	NP_001349860.1:n.694+1027G>A
NM_001362932.1:c.463G>A	NP_001349861.1:p.Ala155Thr
NM_018972.3:c.790G>A	NP_061845.2:p.Ala264Thr
NM_001362931.2:c.694+1027G>A	NP_001349860.1:n.694+1027G>A
NM_018972.4:c.790G>A MANE Select	NP_061845.2:p.Ala264Thr
NM_001040875.4:c.586G>A	NP_001035808.1:p.Ala196Thr
NM_001362929.2:c.463G>A	NP_001349858.1:p.Ala155Thr
NM_001362930.2:c.616G>A	NP_001349859.1:p.Ala206Thr
NM_001362932.2:c.463G>A	NP_001349861.1:p.Ala155Thr