Canonical Allele Identifier: CA351408700

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242690710T>G (hg19) ; chr2:g.241751295T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241751295T>G , CM000664.2:g.241751295T>G	GRCh38
NC_000002.11:g.242690710T>G , CM000664.1:g.242690710T>G	GRCh37
NC_000002.10:g.242339383T>G	NCBI36
NG_012012.1:g.21681T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1047T>G MANE Select	ENSP00000315351.4:p.His349Gln
ENST00000321264.8:c.1047T>G	ENSP00000315351.4:p.His349Gln
ENST00000400769.6:c.854-4554T>G	ENSP00000383580.2:n.854-4554T>G
ENST00000403782.5:c.645T>G	ENSP00000384723.1:p.His215Gln
ENST00000432449.1:c.307T>G
ENST00000436747.5:c.*1363T>G	ENSP00000400212.1:n.*1363T>G
ENST00000454048.1:c.150T>G	ENSP00000404596.1:p.His50Gln
ENST00000467427.5:n.389+1001T>G
ENST00000470343.5:n.528T>G
ENST00000473126.1:n.246T>G
ENST00000486953.5:n.163+1001T>G
ENST00000496252.5:n.402T>G
NM_001287249.1:c.645T>G	NP_001274178.1:p.His215Gln
NM_152783.4:c.1047T>G	NP_689996.4:p.His349Gln
NR_109778.1:n.1063-4554T>G
XM_011511734.1:c.1125T>G	XP_011510036.1:p.His375Gln
XM_011511735.1:c.1125T>G	XP_011510037.1:p.His375Gln
XM_011511736.1:c.1047T>G	XP_011510038.1:p.His349Gln
XM_011511737.1:c.1125T>G	XP_011510039.1:p.His375Gln
XM_011511742.1:c.1262T>G	XP_011510044.1:p.Met421Arg
XM_011511743.1:c.1262T>G	XP_011510045.1:p.Met421Arg
XM_011511744.1:c.1262T>G	XP_011510046.1:p.Met421Arg
XM_011511745.1:c.1125T>G	XP_011510047.1:p.His375Gln
XM_011511748.1:c.1196T>G	XP_011510050.1:p.Met399Arg
XM_011511749.1:c.1179+1001T>G	XP_011510051.1:n.1179+1001T>G
XM_011511750.1:c.1125T>G	XP_011510052.1:p.His375Gln
XM_011511751.1:c.1212+716T>G	XP_011510053.1:n.1212+716T>G
XM_011511753.1:c.1075+1001T>G	XP_011510055.1:n.1075+1001T>G
XM_011511754.1:c.564T>G	XP_011510056.1:p.His188Gln
XM_011511755.1:c.555T>G	XP_011510057.1:p.His185Gln
XM_011511756.1:c.853+6418T>G	XP_011510058.1:n.853+6418T>G
XM_011511757.1:c.*63T>G	XP_011510059.1:n.*63T>G
XR_241434.3:n.1386T>G
XR_923003.1:n.1908T>G
XR_923004.1:n.1679T>G
XR_923005.1:n.1422T>G
XR_923006.1:n.1422T>G
XR_923007.1:n.1389T>G
XR_923008.1:n.1285T>G
XR_923009.1:n.1285T>G
XR_923010.1:n.1719T>G
XR_923011.1:n.1490T>G
XR_923012.1:n.1424T>G
XR_923014.1:n.1014-4554T>G
NM_001352824.1:c.486T>G	NP_001339753.1:p.His162Gln
XM_011511734.2:c.1125T>G	XP_011510036.1:p.His375Gln
XM_011511735.2:c.1125T>G	XP_011510037.1:p.His375Gln
XM_011511736.2:c.1047T>G	XP_011510038.1:p.His349Gln
XM_011511737.3:c.1125T>G	XP_011510039.1:p.His375Gln
XM_011511743.2:c.1262T>G	XP_011510045.1:p.Met421Arg
XM_011511744.2:c.1262T>G	XP_011510046.1:p.Met421Arg
XM_011511745.3:c.1125T>G	XP_011510047.1:p.His375Gln
XM_011511749.3:c.1179+1001T>G	XP_011510051.1:n.1179+1001T>G
XM_011511750.3:c.1125T>G	XP_011510052.1:p.His375Gln
XM_011511751.2:c.1212+716T>G	XP_011510053.1:n.1212+716T>G
XM_011511753.3:c.1075+1001T>G	XP_011510055.1:n.1075+1001T>G
XM_011511756.2:c.853+6418T>G	XP_011510058.1:n.853+6418T>G
XM_011511757.3:c.*63T>G	XP_011510059.1:n.*63T>G
XM_017004828.2:c.1047T>G	XP_016860317.1:p.His349Gln
XM_017004829.2:c.1262T>G	XP_016860318.1:p.Met421Arg
XM_017004830.2:c.1125T>G	XP_016860319.1:p.His375Gln
XM_024453102.1:c.897T>G	XP_024308870.1:p.His299Gln
XR_001738918.2:n.1421T>G
XR_001738919.2:n.1355T>G
XR_002959334.1:n.1907T>G
XR_002959335.1:n.1551T>G
XR_241434.4:n.1385T>G
XR_923004.3:n.1678T>G
XR_923005.2:n.1421T>G
XR_923007.3:n.1388T>G
XR_923009.2:n.1284T>G
XR_923010.2:n.1718T>G
XR_923011.3:n.1489T>G
XR_923012.2:n.1423T>G
XR_923014.3:n.1013-4554T>G
NM_152783.5:c.1047T>G MANE Select	NP_689996.4:p.His349Gln
NM_001287249.2:c.645T>G	NP_001274178.1:p.His215Gln
NM_001352824.2:c.486T>G	NP_001339753.1:p.His162Gln
NR_109778.2:n.1012-4554T>G