Canonical Allele Identifier: CA351408774

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242690744G>T (hg19) ; chr2:g.241751329G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241751329G>T , CM000664.2:g.241751329G>T	GRCh38
NC_000002.11:g.242690744G>T , CM000664.1:g.242690744G>T	GRCh37
NC_000002.10:g.242339417G>T	NCBI36
NG_012012.1:g.21715G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1081G>T MANE Select	ENSP00000315351.4:p.Ala361Ser
ENST00000321264.8:c.1081G>T	ENSP00000315351.4:p.Ala361Ser
ENST00000400769.6:c.854-4520G>T	ENSP00000383580.2:n.854-4520G>T
ENST00000403782.5:c.679G>T	ENSP00000384723.1:p.Ala227Ser
ENST00000432449.1:c.341G>T
ENST00000436747.5:c.*1397G>T	ENSP00000400212.1:n.*1397G>T
ENST00000454048.1:c.184G>T	ENSP00000404596.1:p.Ala62Ser
ENST00000467427.5:n.389+1035G>T
ENST00000470343.5:n.562G>T
ENST00000473126.1:n.280G>T
ENST00000486953.5:n.163+1035G>T
ENST00000496252.5:n.436G>T
NM_001287249.1:c.679G>T	NP_001274178.1:p.Ala227Ser
NM_152783.4:c.1081G>T	NP_689996.4:p.Ala361Ser
NR_109778.1:n.1063-4520G>T
XM_011511734.1:c.1159G>T	XP_011510036.1:p.Ala387Ser
XM_011511735.1:c.1159G>T	XP_011510037.1:p.Ala387Ser
XM_011511736.1:c.1081G>T	XP_011510038.1:p.Ala361Ser
XM_011511737.1:c.1159G>T	XP_011510039.1:p.Ala387Ser
XM_011511742.1:c.1296G>T	XP_011510044.1:p.Thr432=
XM_011511743.1:c.1296G>T	XP_011510045.1:p.Thr432=
XM_011511744.1:c.1296G>T	XP_011510046.1:p.Thr432=
XM_011511745.1:c.1159G>T	XP_011510047.1:p.Ala387Ser
XM_011511748.1:c.1230G>T	XP_011510050.1:p.Thr410=
XM_011511749.1:c.1179+1035G>T	XP_011510051.1:n.1179+1035G>T
XM_011511750.1:c.1159G>T	XP_011510052.1:p.Ala387Ser
XM_011511751.1:c.1212+750G>T	XP_011510053.1:n.1212+750G>T
XM_011511753.1:c.1075+1035G>T	XP_011510055.1:n.1075+1035G>T
XM_011511754.1:c.598G>T	XP_011510056.1:p.Ala200Ser
XM_011511755.1:c.589G>T	XP_011510057.1:p.Ala197Ser
XM_011511756.1:c.853+6452G>T	XP_011510058.1:n.853+6452G>T
XM_011511757.1:c.*97G>T	XP_011510059.1:n.*97G>T
XR_241434.3:n.1420G>T
XR_923003.1:n.1942G>T
XR_923004.1:n.1713G>T
XR_923005.1:n.1456G>T
XR_923006.1:n.1456G>T
XR_923007.1:n.1423G>T
XR_923008.1:n.1319G>T
XR_923009.1:n.1319G>T
XR_923010.1:n.1753G>T
XR_923011.1:n.1524G>T
XR_923012.1:n.1458G>T
XR_923014.1:n.1014-4520G>T
NM_001352824.1:c.520G>T	NP_001339753.1:p.Ala174Ser
XM_011511734.2:c.1159G>T	XP_011510036.1:p.Ala387Ser
XM_011511735.2:c.1159G>T	XP_011510037.1:p.Ala387Ser
XM_011511736.2:c.1081G>T	XP_011510038.1:p.Ala361Ser
XM_011511737.3:c.1159G>T	XP_011510039.1:p.Ala387Ser
XM_011511743.2:c.1296G>T	XP_011510045.1:p.Thr432=
XM_011511744.2:c.1296G>T	XP_011510046.1:p.Thr432=
XM_011511745.3:c.1159G>T	XP_011510047.1:p.Ala387Ser
XM_011511749.3:c.1179+1035G>T	XP_011510051.1:n.1179+1035G>T
XM_011511750.3:c.1159G>T	XP_011510052.1:p.Ala387Ser
XM_011511751.2:c.1212+750G>T	XP_011510053.1:n.1212+750G>T
XM_011511753.3:c.1075+1035G>T	XP_011510055.1:n.1075+1035G>T
XM_011511756.2:c.853+6452G>T	XP_011510058.1:n.853+6452G>T
XM_017004828.2:c.1081G>T	XP_016860317.1:p.Ala361Ser
XM_017004829.2:c.1296G>T	XP_016860318.1:p.Thr432=
XM_017004830.2:c.1159G>T	XP_016860319.1:p.Ala387Ser
XM_024453102.1:c.931G>T	XP_024308870.1:p.Ala311Ser
XR_001738918.2:n.1455G>T
XR_001738919.2:n.1389G>T
XR_002959334.1:n.1941G>T
XR_002959335.1:n.1585G>T
XR_241434.4:n.1419G>T
XR_923004.3:n.1712G>T
XR_923005.2:n.1455G>T
XR_923007.3:n.1422G>T
XR_923009.2:n.1318G>T
XR_923010.2:n.1752G>T
XR_923011.3:n.1523G>T
XR_923012.2:n.1457G>T
XR_923014.3:n.1013-4520G>T
NM_152783.5:c.1081G>T MANE Select	NP_689996.4:p.Ala361Ser
NM_001287249.2:c.679G>T	NP_001274178.1:p.Ala227Ser
NM_001352824.2:c.520G>T	NP_001339753.1:p.Ala174Ser
NR_109778.2:n.1012-4520G>T