Canonical Allele Identifier: CA461772369

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276297C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364062C>T , CM000670.2:g.74364062C>T	GRCh38
NC_000008.10:g.75276297C>T , CM000670.1:g.75276297C>T	GRCh37
NC_000008.9:g.75438852C>T	NCBI36
NG_008787.2:g.47933C>T
NG_008787.3:g.47933C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220822.12:c.772C>T MANE Select	ENSP00000220822.7:p.Leu258=
ENST00000434412.3:c.640C>T	ENSP00000417006.3:p.Leu214=
ENST00000520797.6:n.883C>T
ENST00000521096.6:n.628C>T
ENST00000522568.2:c.*444C>T	ENSP00000430136.1:n.*444C>T
ENST00000523640.2:c.165+12741C>T	ENSP00000502017.1:n.165+12741C>T
ENST00000524195.2:c.280+1009C>T	ENSP00000502308.1:n.280+1009C>T
ENST00000674612.1:c.445C>T	ENSP00000501864.1:p.Leu149=
ENST00000674710.1:c.694+1009C>T	ENSP00000502762.1:n.694+1009C>T
ENST00000674754.1:c.*2335C>T	ENSP00000502063.1:n.*2335C>T
ENST00000674756.1:c.*366+1009C>T	ENSP00000501860.1:n.*366+1009C>T
ENST00000674806.1:c.445C>T	ENSP00000502637.1:p.Leu149=
ENST00000674865.1:c.568C>T	ENSP00000502437.1:p.Leu190=
ENST00000674926.1:c.*1404C>T	ENSP00000501799.1:n.*1404C>T
ENST00000674934.1:c.*460C>T	ENSP00000502187.1:n.*460C>T
ENST00000674944.1:c.*1375C>T	ENSP00000501858.1:n.*1375C>T
ENST00000674946.1:c.694+1009C>T	ENSP00000501569.1:n.694+1009C>T
ENST00000674973.1:c.466C>T	ENSP00000502447.1:p.Leu156=
ENST00000675007.1:c.*510C>T	ENSP00000502119.1:n.*510C>T
ENST00000675060.1:c.*437C>T	ENSP00000501616.1:n.*437C>T
ENST00000675165.1:c.769C>T	ENSP00000502612.1:p.Leu257=
ENST00000675220.1:c.445C>T	ENSP00000502588.1:p.Leu149=
ENST00000675265.1:c.*522C>T	ENSP00000501848.1:n.*522C>T
ENST00000675336.1:c.*258C>T	ENSP00000502120.1:n.*258C>T
ENST00000675376.1:c.445C>T	ENSP00000502838.1:p.Leu149=
ENST00000675463.1:c.850C>T	ENSP00000502327.1:p.Leu284=
ENST00000675472.1:c.*258C>T	ENSP00000501946.1:n.*258C>T
ENST00000675474.1:n.357C>T
ENST00000675560.1:c.*366+1009C>T	ENSP00000502118.1:n.*366+1009C>T
ENST00000675625.1:c.*444C>T	ENSP00000501626.1:n.*444C>T
ENST00000675633.1:c.*179C>T	ENSP00000501785.1:n.*179C>T
ENST00000675661.1:c.*532C>T	ENSP00000501958.1:n.*532C>T
ENST00000675706.1:n.2730C>T
ENST00000675821.1:c.445C>T	ENSP00000502198.1:p.Leu149=
ENST00000675832.1:c.*444C>T	ENSP00000502041.1:n.*444C>T
ENST00000675928.1:c.598C>T	ENSP00000501568.1:p.Leu200=
ENST00000675944.1:c.568C>T	ENSP00000502673.1:p.Leu190=
ENST00000675999.1:c.694+1009C>T	ENSP00000502572.1:n.694+1009C>T
ENST00000676049.1:c.*674C>T	ENSP00000501912.1:n.*674C>T
ENST00000676112.1:c.838C>T	ENSP00000502295.1:p.Leu280=
ENST00000676143.1:c.445C>T	ENSP00000502828.1:p.Leu149=
ENST00000676207.1:c.694+1009C>T	ENSP00000502638.1:n.694+1009C>T
ENST00000676377.1:c.445C>T	ENSP00000502756.1:p.Leu149=
ENST00000676415.1:c.*78C>T	ENSP00000502665.1:n.*78C>T
ENST00000676443.1:c.724C>T	ENSP00000501769.1:p.Leu242=
ENST00000220822.11:c.772C>T	ENSP00000220822.7:p.Leu258=
ENST00000434412.2:c.568C>T	ENSP00000417006.2:p.Leu190=
ENST00000520797.5:n.537C>T
ENST00000521096.5:n.578C>T
ENST00000522568.1:c.*444C>T	ENSP00000430136.1:n.*444C>T
ENST00000524195.1:n.103+1009C>T
NM_001040875.2:c.568C>T	NP_001035808.1:p.Leu190=
NM_018972.2:c.772C>T	NP_061845.2:p.Leu258=
NR_046346.1:n.706C>T
XM_011517551.1:c.1066C>T	XP_011515853.1:p.Leu356=
XM_011517552.1:c.445C>T	XP_011515854.1:p.Leu149=
NM_001040875.3:c.568C>T	NP_001035808.1:p.Leu190=
NM_001362929.1:c.445C>T	NP_001349858.1:p.Leu149=
NM_001362930.1:c.598C>T	NP_001349859.1:p.Leu200=
NM_001362931.1:c.694+1009C>T	NP_001349860.1:n.694+1009C>T
NM_001362932.1:c.445C>T	NP_001349861.1:p.Leu149=
NM_018972.3:c.772C>T	NP_061845.2:p.Leu258=
NM_001362931.2:c.694+1009C>T	NP_001349860.1:n.694+1009C>T
NM_018972.4:c.772C>T MANE Select	NP_061845.2:p.Leu258=
NM_001040875.4:c.568C>T	NP_001035808.1:p.Leu190=
NM_001362929.2:c.445C>T	NP_001349858.1:p.Leu149=
NM_001362930.2:c.598C>T	NP_001349859.1:p.Leu200=
NM_001362932.2:c.445C>T	NP_001349861.1:p.Leu149=