Canonical Allele Identifier: CA371550369

Gene: GDAP1

Linked Data

• MyVariant Identifiers: chr8:g.75276365C>G (hg19) ; chr8:g.74364130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74364130C>G , CM000670.2:g.74364130C>G	GRCh38
NC_000008.10:g.75276365C>G , CM000670.1:g.75276365C>G	GRCh37
NC_000008.9:g.75438920C>G	NCBI36
NG_008787.2:g.48001C>G
NG_008787.3:g.48001C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220822.12:c.840C>G MANE Select	ENSP00000220822.7:p.Tyr280Ter
ENST00000434412.3:c.708C>G	ENSP00000417006.3:p.Tyr236Ter
ENST00000520797.6:n.951C>G
ENST00000521096.6:n.696C>G
ENST00000522568.2:c.*512C>G	ENSP00000430136.1:n.*512C>G
ENST00000523640.2:c.165+12809C>G	ENSP00000502017.1:n.165+12809C>G
ENST00000524195.2:c.280+1077C>G	ENSP00000502308.1:n.280+1077C>G
ENST00000674612.1:c.513C>G	ENSP00000501864.1:p.Tyr171Ter
ENST00000674710.1:c.694+1077C>G	ENSP00000502762.1:n.694+1077C>G
ENST00000674754.1:c.*2403C>G	ENSP00000502063.1:n.*2403C>G
ENST00000674756.1:c.*366+1077C>G	ENSP00000501860.1:n.*366+1077C>G
ENST00000674806.1:c.513C>G	ENSP00000502637.1:p.Tyr171Ter
ENST00000674865.1:c.636C>G	ENSP00000502437.1:p.Tyr212Ter
ENST00000674926.1:c.*1472C>G	ENSP00000501799.1:n.*1472C>G
ENST00000674934.1:c.*528C>G	ENSP00000502187.1:n.*528C>G
ENST00000674944.1:c.*1443C>G	ENSP00000501858.1:n.*1443C>G
ENST00000674946.1:c.694+1077C>G	ENSP00000501569.1:n.694+1077C>G
ENST00000674973.1:c.534C>G	ENSP00000502447.1:p.Tyr178Ter
ENST00000675007.1:c.*578C>G	ENSP00000502119.1:n.*578C>G
ENST00000675060.1:c.*505C>G	ENSP00000501616.1:n.*505C>G
ENST00000675165.1:c.837C>G	ENSP00000502612.1:p.Tyr279Ter
ENST00000675220.1:c.513C>G	ENSP00000502588.1:p.Tyr171Ter
ENST00000675265.1:c.*590C>G	ENSP00000501848.1:n.*590C>G
ENST00000675336.1:c.*326C>G	ENSP00000502120.1:n.*326C>G
ENST00000675376.1:c.513C>G	ENSP00000502838.1:p.Tyr171Ter
ENST00000675463.1:c.918C>G	ENSP00000502327.1:p.Tyr306Ter
ENST00000675472.1:c.*326C>G	ENSP00000501946.1:n.*326C>G
ENST00000675474.1:n.425C>G
ENST00000675560.1:c.*366+1077C>G	ENSP00000502118.1:n.*366+1077C>G
ENST00000675625.1:c.*512C>G	ENSP00000501626.1:n.*512C>G
ENST00000675633.1:c.*247C>G	ENSP00000501785.1:n.*247C>G
ENST00000675661.1:c.*600C>G	ENSP00000501958.1:n.*600C>G
ENST00000675706.1:n.2798C>G
ENST00000675821.1:c.513C>G	ENSP00000502198.1:p.Tyr171Ter
ENST00000675832.1:c.*512C>G	ENSP00000502041.1:n.*512C>G
ENST00000675928.1:c.666C>G	ENSP00000501568.1:p.Tyr222Ter
ENST00000675944.1:c.636C>G	ENSP00000502673.1:p.Tyr212Ter
ENST00000675999.1:c.694+1077C>G	ENSP00000502572.1:n.694+1077C>G
ENST00000676049.1:c.*742C>G	ENSP00000501912.1:n.*742C>G
ENST00000676112.1:c.906C>G	ENSP00000502295.1:p.Tyr302Ter
ENST00000676143.1:c.513C>G	ENSP00000502828.1:p.Tyr171Ter
ENST00000676207.1:c.694+1077C>G	ENSP00000502638.1:n.694+1077C>G
ENST00000676377.1:c.513C>G	ENSP00000502756.1:p.Tyr171Ter
ENST00000676415.1:c.*146C>G	ENSP00000502665.1:n.*146C>G
ENST00000676443.1:c.792C>G	ENSP00000501769.1:p.Tyr264Ter
ENST00000220822.11:c.840C>G	ENSP00000220822.7:p.Tyr280Ter
ENST00000434412.2:c.636C>G	ENSP00000417006.2:p.Tyr212Ter
ENST00000520797.5:n.605C>G
ENST00000521096.5:n.646C>G
ENST00000522568.1:c.*512C>G	ENSP00000430136.1:n.*512C>G
ENST00000524195.1:n.103+1077C>G
NM_001040875.2:c.636C>G	NP_001035808.1:p.Tyr212Ter
NM_018972.2:c.840C>G	NP_061845.2:p.Tyr280Ter
NR_046346.1:n.774C>G
XM_011517551.1:c.1134C>G	XP_011515853.1:p.Tyr378Ter
XM_011517552.1:c.513C>G	XP_011515854.1:p.Tyr171Ter
NM_001040875.3:c.636C>G	NP_001035808.1:p.Tyr212Ter
NM_001362929.1:c.513C>G	NP_001349858.1:p.Tyr171Ter
NM_001362930.1:c.666C>G	NP_001349859.1:p.Tyr222Ter
NM_001362931.1:c.694+1077C>G	NP_001349860.1:n.694+1077C>G
NM_001362932.1:c.513C>G	NP_001349861.1:p.Tyr171Ter
NM_018972.3:c.840C>G	NP_061845.2:p.Tyr280Ter
NM_001362931.2:c.694+1077C>G	NP_001349860.1:n.694+1077C>G
NM_018972.4:c.840C>G MANE Select	NP_061845.2:p.Tyr280Ter
NM_001040875.4:c.636C>G	NP_001035808.1:p.Tyr212Ter
NM_001362929.2:c.513C>G	NP_001349858.1:p.Tyr171Ter
NM_001362930.2:c.666C>G	NP_001349859.1:p.Tyr222Ter
NM_001362932.2:c.513C>G	NP_001349861.1:p.Tyr171Ter