Canonical Allele Identifier: CA351408608

Gene: D2HGDH

Linked Data

• dbSNP Id: rs1697147190
• gnomAD v3: 2-241751250-T-A
• gnomAD v4: 2-241751250-T-A
• MyVariant Identifiers: chr2:g.242690665T>A (hg19) ; chr2:g.241751250T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241751250T>A , CM000664.2:g.241751250T>A	GRCh38
NC_000002.11:g.242690665T>A , CM000664.1:g.242690665T>A	GRCh37
NC_000002.10:g.242339338T>A	NCBI36
NG_012012.1:g.21636T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1002T>A MANE Select	ENSP00000315351.4:p.Ser334Arg
ENST00000321264.8:c.1002T>A	ENSP00000315351.4:p.Ser334Arg
ENST00000400769.6:c.854-4599T>A	ENSP00000383580.2:n.854-4599T>A
ENST00000403782.5:c.600T>A	ENSP00000384723.1:p.Ser200Arg
ENST00000432449.1:c.262T>A
ENST00000436747.5:c.*1318T>A	ENSP00000400212.1:n.*1318T>A
ENST00000454048.1:c.105T>A	ENSP00000404596.1:p.Ser35Arg
ENST00000467427.5:n.389+956T>A
ENST00000470343.5:n.483T>A
ENST00000473126.1:n.201T>A
ENST00000486953.5:n.163+956T>A
ENST00000496252.5:n.357T>A
NM_001287249.1:c.600T>A	NP_001274178.1:p.Ser200Arg
NM_152783.4:c.1002T>A	NP_689996.4:p.Ser334Arg
NR_109778.1:n.1063-4599T>A
XM_011511734.1:c.1080T>A	XP_011510036.1:p.Ser360Arg
XM_011511735.1:c.1080T>A	XP_011510037.1:p.Ser360Arg
XM_011511736.1:c.1002T>A	XP_011510038.1:p.Ser334Arg
XM_011511737.1:c.1080T>A	XP_011510039.1:p.Ser360Arg
XM_011511742.1:c.1217T>A	XP_011510044.1:p.Val406Asp
XM_011511743.1:c.1217T>A	XP_011510045.1:p.Val406Asp
XM_011511744.1:c.1217T>A	XP_011510046.1:p.Val406Asp
XM_011511745.1:c.1080T>A	XP_011510047.1:p.Ser360Arg
XM_011511748.1:c.1151T>A	XP_011510050.1:p.Val384Asp
XM_011511749.1:c.1179+956T>A	XP_011510051.1:n.1179+956T>A
XM_011511750.1:c.1080T>A	XP_011510052.1:p.Ser360Arg
XM_011511751.1:c.1212+671T>A	XP_011510053.1:n.1212+671T>A
XM_011511753.1:c.1075+956T>A	XP_011510055.1:n.1075+956T>A
XM_011511754.1:c.519T>A	XP_011510056.1:p.Ser173Arg
XM_011511755.1:c.510T>A	XP_011510057.1:p.Ser170Arg
XM_011511756.1:c.853+6373T>A	XP_011510058.1:n.853+6373T>A
XM_011511757.1:c.*18T>A	XP_011510059.1:n.*18T>A
XR_241434.3:n.1341T>A
XR_923003.1:n.1863T>A
XR_923004.1:n.1634T>A
XR_923005.1:n.1377T>A
XR_923006.1:n.1377T>A
XR_923007.1:n.1344T>A
XR_923008.1:n.1240T>A
XR_923009.1:n.1240T>A
XR_923010.1:n.1674T>A
XR_923011.1:n.1445T>A
XR_923012.1:n.1379T>A
XR_923014.1:n.1014-4599T>A
NM_001352824.1:c.441T>A	NP_001339753.1:p.Ser147Arg
XM_011511734.2:c.1080T>A	XP_011510036.1:p.Ser360Arg
XM_011511735.2:c.1080T>A	XP_011510037.1:p.Ser360Arg
XM_011511736.2:c.1002T>A	XP_011510038.1:p.Ser334Arg
XM_011511737.3:c.1080T>A	XP_011510039.1:p.Ser360Arg
XM_011511743.2:c.1217T>A	XP_011510045.1:p.Val406Asp
XM_011511744.2:c.1217T>A	XP_011510046.1:p.Val406Asp
XM_011511745.3:c.1080T>A	XP_011510047.1:p.Ser360Arg
XM_011511749.3:c.1179+956T>A	XP_011510051.1:n.1179+956T>A
XM_011511750.3:c.1080T>A	XP_011510052.1:p.Ser360Arg
XM_011511751.2:c.1212+671T>A	XP_011510053.1:n.1212+671T>A
XM_011511753.3:c.1075+956T>A	XP_011510055.1:n.1075+956T>A
XM_011511756.2:c.853+6373T>A	XP_011510058.1:n.853+6373T>A
XM_011511757.3:c.*18T>A	XP_011510059.1:n.*18T>A
XM_017004828.2:c.1002T>A	XP_016860317.1:p.Ser334Arg
XM_017004829.2:c.1217T>A	XP_016860318.1:p.Val406Asp
XM_017004830.2:c.1080T>A	XP_016860319.1:p.Ser360Arg
XM_024453102.1:c.852T>A	XP_024308870.1:p.Ser284Arg
XR_001738918.2:n.1376T>A
XR_001738919.2:n.1310T>A
XR_002959334.1:n.1862T>A
XR_002959335.1:n.1506T>A
XR_241434.4:n.1340T>A
XR_923004.3:n.1633T>A
XR_923005.2:n.1376T>A
XR_923007.3:n.1343T>A
XR_923009.2:n.1239T>A
XR_923010.2:n.1673T>A
XR_923011.3:n.1444T>A
XR_923012.2:n.1378T>A
XR_923014.3:n.1013-4599T>A
NM_152783.5:c.1002T>A MANE Select	NP_689996.4:p.Ser334Arg
NM_001287249.2:c.600T>A	NP_001274178.1:p.Ser200Arg
NM_001352824.2:c.441T>A	NP_001339753.1:p.Ser147Arg
NR_109778.2:n.1012-4599T>A