Canonical Allele Identifier: CA351408615

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242690669T>C (hg19) ; chr2:g.241751254T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241751254T>C , CM000664.2:g.241751254T>C	GRCh38
NC_000002.11:g.242690669T>C , CM000664.1:g.242690669T>C	GRCh37
NC_000002.10:g.242339342T>C	NCBI36
NG_012012.1:g.21640T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1006T>C MANE Select	ENSP00000315351.4:p.Phe336Leu
ENST00000321264.8:c.1006T>C	ENSP00000315351.4:p.Phe336Leu
ENST00000400769.6:c.854-4595T>C	ENSP00000383580.2:n.854-4595T>C
ENST00000403782.5:c.604T>C	ENSP00000384723.1:p.Phe202Leu
ENST00000432449.1:c.266T>C
ENST00000436747.5:c.*1322T>C	ENSP00000400212.1:n.*1322T>C
ENST00000454048.1:c.109T>C	ENSP00000404596.1:p.Phe37Leu
ENST00000467427.5:n.389+960T>C
ENST00000470343.5:n.487T>C
ENST00000473126.1:n.205T>C
ENST00000486953.5:n.163+960T>C
ENST00000496252.5:n.361T>C
NM_001287249.1:c.604T>C	NP_001274178.1:p.Phe202Leu
NM_152783.4:c.1006T>C	NP_689996.4:p.Phe336Leu
NR_109778.1:n.1063-4595T>C
XM_011511734.1:c.1084T>C	XP_011510036.1:p.Phe362Leu
XM_011511735.1:c.1084T>C	XP_011510037.1:p.Phe362Leu
XM_011511736.1:c.1006T>C	XP_011510038.1:p.Phe336Leu
XM_011511737.1:c.1084T>C	XP_011510039.1:p.Phe362Leu
XM_011511742.1:c.1221T>C	XP_011510044.1:p.Arg407=
XM_011511743.1:c.1221T>C	XP_011510045.1:p.Arg407=
XM_011511744.1:c.1221T>C	XP_011510046.1:p.Arg407=
XM_011511745.1:c.1084T>C	XP_011510047.1:p.Phe362Leu
XM_011511748.1:c.1155T>C	XP_011510050.1:p.Arg385=
XM_011511749.1:c.1179+960T>C	XP_011510051.1:n.1179+960T>C
XM_011511750.1:c.1084T>C	XP_011510052.1:p.Phe362Leu
XM_011511751.1:c.1212+675T>C	XP_011510053.1:n.1212+675T>C
XM_011511753.1:c.1075+960T>C	XP_011510055.1:n.1075+960T>C
XM_011511754.1:c.523T>C	XP_011510056.1:p.Phe175Leu
XM_011511755.1:c.514T>C	XP_011510057.1:p.Phe172Leu
XM_011511756.1:c.853+6377T>C	XP_011510058.1:n.853+6377T>C
XM_011511757.1:c.*22T>C	XP_011510059.1:n.*22T>C
XR_241434.3:n.1345T>C
XR_923003.1:n.1867T>C
XR_923004.1:n.1638T>C
XR_923005.1:n.1381T>C
XR_923006.1:n.1381T>C
XR_923007.1:n.1348T>C
XR_923008.1:n.1244T>C
XR_923009.1:n.1244T>C
XR_923010.1:n.1678T>C
XR_923011.1:n.1449T>C
XR_923012.1:n.1383T>C
XR_923014.1:n.1014-4595T>C
NM_001352824.1:c.445T>C	NP_001339753.1:p.Phe149Leu
XM_011511734.2:c.1084T>C	XP_011510036.1:p.Phe362Leu
XM_011511735.2:c.1084T>C	XP_011510037.1:p.Phe362Leu
XM_011511736.2:c.1006T>C	XP_011510038.1:p.Phe336Leu
XM_011511737.3:c.1084T>C	XP_011510039.1:p.Phe362Leu
XM_011511743.2:c.1221T>C	XP_011510045.1:p.Arg407=
XM_011511744.2:c.1221T>C	XP_011510046.1:p.Arg407=
XM_011511745.3:c.1084T>C	XP_011510047.1:p.Phe362Leu
XM_011511749.3:c.1179+960T>C	XP_011510051.1:n.1179+960T>C
XM_011511750.3:c.1084T>C	XP_011510052.1:p.Phe362Leu
XM_011511751.2:c.1212+675T>C	XP_011510053.1:n.1212+675T>C
XM_011511753.3:c.1075+960T>C	XP_011510055.1:n.1075+960T>C
XM_011511756.2:c.853+6377T>C	XP_011510058.1:n.853+6377T>C
XM_011511757.3:c.*22T>C	XP_011510059.1:n.*22T>C
XM_017004828.2:c.1006T>C	XP_016860317.1:p.Phe336Leu
XM_017004829.2:c.1221T>C	XP_016860318.1:p.Arg407=
XM_017004830.2:c.1084T>C	XP_016860319.1:p.Phe362Leu
XM_024453102.1:c.856T>C	XP_024308870.1:p.Phe286Leu
XR_001738918.2:n.1380T>C
XR_001738919.2:n.1314T>C
XR_002959334.1:n.1866T>C
XR_002959335.1:n.1510T>C
XR_241434.4:n.1344T>C
XR_923004.3:n.1637T>C
XR_923005.2:n.1380T>C
XR_923007.3:n.1347T>C
XR_923009.2:n.1243T>C
XR_923010.2:n.1677T>C
XR_923011.3:n.1448T>C
XR_923012.2:n.1382T>C
XR_923014.3:n.1013-4595T>C
NM_152783.5:c.1006T>C MANE Select	NP_689996.4:p.Phe336Leu
NM_001287249.2:c.604T>C	NP_001274178.1:p.Phe202Leu
NM_001352824.2:c.445T>C	NP_001339753.1:p.Phe149Leu
NR_109778.2:n.1012-4595T>C