Canonical Allele Identifier: CA2664134449

Gene: D2HGDH

Linked Data

• gnomAD v4: 2-241767561-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241767561G>A , CM000664.2:g.241767561G>A	GRCh38
NC_000002.11:g.242706976G>A , CM000664.1:g.242706976G>A	GRCh37
NC_000002.10:g.242355649G>A	NCBI36
NG_012012.1:g.37947G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1307-149G>A MANE Select	ENSP00000315351.4:n.1307-149G>A
ENST00000321264.8:c.1307-149G>A	ENSP00000315351.4:n.1307-149G>A
ENST00000400769.6:c.*57-149G>A	ENSP00000383580.2:n.*57-149G>A
ENST00000403782.5:c.905-149G>A	ENSP00000384723.1:n.905-149G>A
ENST00000436747.5:c.*2543-149G>A	ENSP00000400212.1:n.*2543-149G>A
ENST00000445308.1:c.703-149G>A
ENST00000468064.5:n.1197-149G>A
ENST00000470343.5:n.788-149G>A
ENST00000473126.1:n.506-149G>A
ENST00000486953.5:n.1134-152G>A
ENST00000610344.1:c.*151-149G>A	ENSP00000481906.1:n.*151-149G>A
NM_001287249.1:c.905-149G>A	NP_001274178.1:n.905-149G>A
NM_152783.4:c.1307-149G>A	NP_689996.4:n.1307-149G>A
NR_109778.1:n.1229-149G>A
XM_011511734.1:c.1427-149G>A	XP_011510036.1:n.1427-149G>A
XM_011511735.1:c.1385-149G>A	XP_011510037.1:n.1385-149G>A
XM_011511736.1:c.1349-149G>A	XP_011510038.1:n.1349-149G>A
XM_011511744.1:c.*39-149G>A	XP_011510046.1:n.*39-149G>A
XM_011511750.1:c.1219-149G>A	XP_011510052.1:n.1219-149G>A
XM_011511754.1:c.866-149G>A	XP_011510056.1:n.866-149G>A
XM_011511755.1:c.857-149G>A	XP_011510057.1:n.857-149G>A
XM_011511756.1:c.854-149G>A	XP_011510058.1:n.854-149G>A
XR_923004.1:n.1939-149G>A
XR_923007.1:n.1649-149G>A
XR_923011.1:n.1750-149G>A
NM_001352824.1:c.746-149G>A	NP_001339753.1:n.746-149G>A
XM_011511734.2:c.1427-149G>A	XP_011510036.1:n.1427-149G>A
XM_011511735.2:c.1385-149G>A	XP_011510037.1:n.1385-149G>A
XM_011511736.2:c.1349-149G>A	XP_011510038.1:n.1349-149G>A
XM_011511744.2:c.*39-149G>A	XP_011510046.1:n.*39-149G>A
XM_011511750.3:c.1219-149G>A	XP_011510052.1:n.1219-149G>A
XM_011511756.2:c.854-149G>A	XP_011510058.1:n.854-149G>A
XM_024453102.1:c.1199-149G>A	XP_024308870.1:n.1199-149G>A
XR_001738918.2:n.1681-149G>A
XR_001738919.2:n.1615-149G>A
XR_923004.3:n.1938-149G>A
XR_923007.3:n.1648-149G>A
XR_923011.3:n.1749-149G>A
NM_152783.5:c.1307-149G>A MANE Select	NP_689996.4:n.1307-149G>A
NM_001287249.2:c.905-149G>A	NP_001274178.1:n.905-149G>A
NM_001352824.2:c.746-149G>A	NP_001339753.1:n.746-149G>A
NR_109778.2:n.1178-149G>A