Canonical Allele Identifier: CA1044149538
Gene: D2HGDH HGNC NCBI

Linked Data

dbSNP Id: rs1697115960

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241751133_241751135del , CM000664.2:g.241751133_241751135del GRCh38
NC_000002.11:g.242690548_242690550del , CM000664.1:g.242690548_242690550del GRCh37
NC_000002.10:g.242339221_242339223del NCBI36
NG_012012.1:g.21519_21521del

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.998-113_998-111del MANE Select ENSP00000315351.4:n.998-113_998-111del
ENST00000321264.8:c.998-113_998-111del ENSP00000315351.4:n.998-113_998-111del
ENST00000400769.6:c.854-4716_854-4714del ENSP00000383580.2:n.854-4716_854-4714del
ENST00000403782.5:c.596-113_596-111del ENSP00000384723.1:n.596-113_596-111del
ENST00000432449.1:c.258-113_258-111del
ENST00000436747.5:c.*1314-113_*1314-111del ENSP00000400212.1:n.*1314-113_*1314-111del
ENST00000454048.1:c.101-113_101-111del ENSP00000404596.1:n.101-113_101-111del
ENST00000467427.5:n.389+839_389+841del
ENST00000470343.5:n.479-113_479-111del
ENST00000473126.1:n.197-113_197-111del
ENST00000486953.5:n.163+839_163+841del
ENST00000496252.5:n.353-113_353-111del
NM_001287249.1:c.596-113_596-111del NP_001274178.1:n.596-113_596-111del
NM_152783.4:c.998-113_998-111del NP_689996.4:n.998-113_998-111del
NR_109778.1:n.1063-4716_1063-4714del
XM_011511734.1:c.1076-113_1076-111del XP_011510036.1:n.1076-113_1076-111del
XM_011511735.1:c.1076-113_1076-111del XP_011510037.1:n.1076-113_1076-111del
XM_011511736.1:c.998-113_998-111del XP_011510038.1:n.998-113_998-111del
XM_011511737.1:c.1076-113_1076-111del XP_011510039.1:n.1076-113_1076-111del
XM_011511742.1:c.1213-113_1213-111del XP_011510044.1:n.1213-113_1213-111del
XM_011511743.1:c.1213-113_1213-111del XP_011510045.1:n.1213-113_1213-111del
XM_011511744.1:c.1213-113_1213-111del XP_011510046.1:n.1213-113_1213-111del
XM_011511745.1:c.1076-113_1076-111del XP_011510047.1:n.1076-113_1076-111del
XM_011511748.1:c.1147-113_1147-111del XP_011510050.1:n.1147-113_1147-111del
XM_011511749.1:c.1179+839_1179+841del XP_011510051.1:n.1179+839_1179+841del
XM_011511750.1:c.1076-113_1076-111del XP_011510052.1:n.1076-113_1076-111del
XM_011511751.1:c.1212+554_1212+556del XP_011510053.1:n.1212+554_1212+556del
XM_011511753.1:c.1075+839_1075+841del XP_011510055.1:n.1075+839_1075+841del
XM_011511754.1:c.515-113_515-111del XP_011510056.1:n.515-113_515-111del
XM_011511755.1:c.506-113_506-111del XP_011510057.1:n.506-113_506-111del
XM_011511756.1:c.853+6256_853+6258del XP_011510058.1:n.853+6256_853+6258del
XM_011511757.1:c.*14-113_*14-111del XP_011510059.1:n.*14-113_*14-111del
XR_241434.3:n.1337-113_1337-111del
XR_923003.1:n.1859-113_1859-111del
XR_923004.1:n.1630-113_1630-111del
XR_923005.1:n.1373-113_1373-111del
XR_923006.1:n.1373-113_1373-111del
XR_923007.1:n.1340-113_1340-111del
XR_923008.1:n.1236-113_1236-111del
XR_923009.1:n.1236-113_1236-111del
XR_923010.1:n.1670-113_1670-111del
XR_923011.1:n.1441-113_1441-111del
XR_923012.1:n.1375-113_1375-111del
XR_923014.1:n.1014-4716_1014-4714del
NM_001352824.1:c.437-113_437-111del NP_001339753.1:n.437-113_437-111del
XM_011511734.2:c.1076-113_1076-111del XP_011510036.1:n.1076-113_1076-111del
XM_011511735.2:c.1076-113_1076-111del XP_011510037.1:n.1076-113_1076-111del
XM_011511736.2:c.998-113_998-111del XP_011510038.1:n.998-113_998-111del
XM_011511737.3:c.1076-113_1076-111del XP_011510039.1:n.1076-113_1076-111del
XM_011511743.2:c.1213-113_1213-111del XP_011510045.1:n.1213-113_1213-111del
XM_011511744.2:c.1213-113_1213-111del XP_011510046.1:n.1213-113_1213-111del
XM_011511745.3:c.1076-113_1076-111del XP_011510047.1:n.1076-113_1076-111del
XM_011511749.3:c.1179+839_1179+841del XP_011510051.1:n.1179+839_1179+841del
XM_011511750.3:c.1076-113_1076-111del XP_011510052.1:n.1076-113_1076-111del
XM_011511751.2:c.1212+554_1212+556del XP_011510053.1:n.1212+554_1212+556del
XM_011511753.3:c.1075+839_1075+841del XP_011510055.1:n.1075+839_1075+841del
XM_011511756.2:c.853+6256_853+6258del XP_011510058.1:n.853+6256_853+6258del
XM_011511757.3:c.*14-113_*14-111del XP_011510059.1:n.*14-113_*14-111del
XM_017004828.2:c.998-113_998-111del XP_016860317.1:n.998-113_998-111del
XM_017004829.2:c.1213-113_1213-111del XP_016860318.1:n.1213-113_1213-111del
XM_017004830.2:c.1076-113_1076-111del XP_016860319.1:n.1076-113_1076-111del
XM_024453102.1:c.848-113_848-111del XP_024308870.1:n.848-113_848-111del
XR_001738918.2:n.1372-113_1372-111del
XR_001738919.2:n.1306-113_1306-111del
XR_002959334.1:n.1858-113_1858-111del
XR_002959335.1:n.1502-113_1502-111del
XR_241434.4:n.1336-113_1336-111del
XR_923004.3:n.1629-113_1629-111del
XR_923005.2:n.1372-113_1372-111del
XR_923007.3:n.1339-113_1339-111del
XR_923009.2:n.1235-113_1235-111del
XR_923010.2:n.1669-113_1669-111del
XR_923011.3:n.1440-113_1440-111del
XR_923012.2:n.1374-113_1374-111del
XR_923014.3:n.1013-4716_1013-4714del
NM_152783.5:c.998-113_998-111del MANE Select NP_689996.4:n.998-113_998-111del
NM_001287249.2:c.596-113_596-111del NP_001274178.1:n.596-113_596-111del
NM_001352824.2:c.437-113_437-111del NP_001339753.1:n.437-113_437-111del
NR_109778.2:n.1012-4716_1012-4714del