Canonical Allele Identifier: CA351408624

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242690672T>G (hg19) ; chr2:g.241751257T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241751257T>G , CM000664.2:g.241751257T>G	GRCh38
NC_000002.11:g.242690672T>G , CM000664.1:g.242690672T>G	GRCh37
NC_000002.10:g.242339345T>G	NCBI36
NG_012012.1:g.21643T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1009T>G MANE Select	ENSP00000315351.4:p.Tyr337Asp
ENST00000321264.8:c.1009T>G	ENSP00000315351.4:p.Tyr337Asp
ENST00000400769.6:c.854-4592T>G	ENSP00000383580.2:n.854-4592T>G
ENST00000403782.5:c.607T>G	ENSP00000384723.1:p.Tyr203Asp
ENST00000432449.1:c.269T>G
ENST00000436747.5:c.*1325T>G	ENSP00000400212.1:n.*1325T>G
ENST00000454048.1:c.112T>G	ENSP00000404596.1:p.Tyr38Asp
ENST00000467427.5:n.389+963T>G
ENST00000470343.5:n.490T>G
ENST00000473126.1:n.208T>G
ENST00000486953.5:n.163+963T>G
ENST00000496252.5:n.364T>G
NM_001287249.1:c.607T>G	NP_001274178.1:p.Tyr203Asp
NM_152783.4:c.1009T>G	NP_689996.4:p.Tyr337Asp
NR_109778.1:n.1063-4592T>G
XM_011511734.1:c.1087T>G	XP_011510036.1:p.Tyr363Asp
XM_011511735.1:c.1087T>G	XP_011510037.1:p.Tyr363Asp
XM_011511736.1:c.1009T>G	XP_011510038.1:p.Tyr337Asp
XM_011511737.1:c.1087T>G	XP_011510039.1:p.Tyr363Asp
XM_011511742.1:c.1224T>G	XP_011510044.1:p.Phe408Leu
XM_011511743.1:c.1224T>G	XP_011510045.1:p.Phe408Leu
XM_011511744.1:c.1224T>G	XP_011510046.1:p.Phe408Leu
XM_011511745.1:c.1087T>G	XP_011510047.1:p.Tyr363Asp
XM_011511748.1:c.1158T>G	XP_011510050.1:p.Phe386Leu
XM_011511749.1:c.1179+963T>G	XP_011510051.1:n.1179+963T>G
XM_011511750.1:c.1087T>G	XP_011510052.1:p.Tyr363Asp
XM_011511751.1:c.1212+678T>G	XP_011510053.1:n.1212+678T>G
XM_011511753.1:c.1075+963T>G	XP_011510055.1:n.1075+963T>G
XM_011511754.1:c.526T>G	XP_011510056.1:p.Tyr176Asp
XM_011511755.1:c.517T>G	XP_011510057.1:p.Tyr173Asp
XM_011511756.1:c.853+6380T>G	XP_011510058.1:n.853+6380T>G
XM_011511757.1:c.*25T>G	XP_011510059.1:n.*25T>G
XR_241434.3:n.1348T>G
XR_923003.1:n.1870T>G
XR_923004.1:n.1641T>G
XR_923005.1:n.1384T>G
XR_923006.1:n.1384T>G
XR_923007.1:n.1351T>G
XR_923008.1:n.1247T>G
XR_923009.1:n.1247T>G
XR_923010.1:n.1681T>G
XR_923011.1:n.1452T>G
XR_923012.1:n.1386T>G
XR_923014.1:n.1014-4592T>G
NM_001352824.1:c.448T>G	NP_001339753.1:p.Tyr150Asp
XM_011511734.2:c.1087T>G	XP_011510036.1:p.Tyr363Asp
XM_011511735.2:c.1087T>G	XP_011510037.1:p.Tyr363Asp
XM_011511736.2:c.1009T>G	XP_011510038.1:p.Tyr337Asp
XM_011511737.3:c.1087T>G	XP_011510039.1:p.Tyr363Asp
XM_011511743.2:c.1224T>G	XP_011510045.1:p.Phe408Leu
XM_011511744.2:c.1224T>G	XP_011510046.1:p.Phe408Leu
XM_011511745.3:c.1087T>G	XP_011510047.1:p.Tyr363Asp
XM_011511749.3:c.1179+963T>G	XP_011510051.1:n.1179+963T>G
XM_011511750.3:c.1087T>G	XP_011510052.1:p.Tyr363Asp
XM_011511751.2:c.1212+678T>G	XP_011510053.1:n.1212+678T>G
XM_011511753.3:c.1075+963T>G	XP_011510055.1:n.1075+963T>G
XM_011511756.2:c.853+6380T>G	XP_011510058.1:n.853+6380T>G
XM_011511757.3:c.*25T>G	XP_011510059.1:n.*25T>G
XM_017004828.2:c.1009T>G	XP_016860317.1:p.Tyr337Asp
XM_017004829.2:c.1224T>G	XP_016860318.1:p.Phe408Leu
XM_017004830.2:c.1087T>G	XP_016860319.1:p.Tyr363Asp
XM_024453102.1:c.859T>G	XP_024308870.1:p.Tyr287Asp
XR_001738918.2:n.1383T>G
XR_001738919.2:n.1317T>G
XR_002959334.1:n.1869T>G
XR_002959335.1:n.1513T>G
XR_241434.4:n.1347T>G
XR_923004.3:n.1640T>G
XR_923005.2:n.1383T>G
XR_923007.3:n.1350T>G
XR_923009.2:n.1246T>G
XR_923010.2:n.1680T>G
XR_923011.3:n.1451T>G
XR_923012.2:n.1385T>G
XR_923014.3:n.1013-4592T>G
NM_152783.5:c.1009T>G MANE Select	NP_689996.4:p.Tyr337Asp
NM_001287249.2:c.607T>G	NP_001274178.1:p.Tyr203Asp
NM_001352824.2:c.448T>G	NP_001339753.1:p.Tyr150Asp
NR_109778.2:n.1012-4592T>G