Canonical Allele Identifier: CA351412907

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242707134A>T (hg19) ; chr2:g.241767719A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241767719A>T , CM000664.2:g.241767719A>T	GRCh38
NC_000002.11:g.242707134A>T , CM000664.1:g.242707134A>T	GRCh37
NC_000002.10:g.242355807A>T	NCBI36
NG_012012.1:g.38105A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000321264.9:c.1316A>T MANE Select	ENSP00000315351.4:p.Asn439Ile
ENST00000321264.8:c.1316A>T	ENSP00000315351.4:p.Asn439Ile
ENST00000400769.6:c.*66A>T	ENSP00000383580.2:n.*66A>T
ENST00000403782.5:c.914A>T	ENSP00000384723.1:p.Asn305Ile
ENST00000436747.5:c.*2552A>T	ENSP00000400212.1:n.*2552A>T
ENST00000445308.1:c.712A>T
ENST00000468064.5:n.1206A>T
ENST00000470343.5:n.797A>T
ENST00000473126.1:n.515A>T
ENST00000486953.5:n.1140A>T
ENST00000610344.1:c.*160A>T	ENSP00000481906.1:n.*160A>T
NM_001287249.1:c.914A>T	NP_001274178.1:p.Asn305Ile
NM_152783.4:c.1316A>T	NP_689996.4:p.Asn439Ile
NR_109778.1:n.1238A>T
XM_011511734.1:c.1436A>T	XP_011510036.1:p.Asn479Ile
XM_011511735.1:c.1394A>T	XP_011510037.1:p.Asn465Ile
XM_011511736.1:c.1358A>T	XP_011510038.1:p.Asn453Ile
XM_011511744.1:c.*48A>T	XP_011510046.1:n.*48A>T
XM_011511750.1:c.1228A>T	XP_011510052.1:p.Thr410Ser
XM_011511754.1:c.875A>T	XP_011510056.1:p.Asn292Ile
XM_011511755.1:c.866A>T	XP_011510057.1:p.Asn289Ile
XM_011511756.1:c.863A>T	XP_011510058.1:p.Asn288Ile
XR_923004.1:n.1948A>T
XR_923007.1:n.1658A>T
XR_923011.1:n.1759A>T
NM_001352824.1:c.755A>T	NP_001339753.1:p.Asn252Ile
XM_011511734.2:c.1436A>T	XP_011510036.1:p.Asn479Ile
XM_011511735.2:c.1394A>T	XP_011510037.1:p.Asn465Ile
XM_011511736.2:c.1358A>T	XP_011510038.1:p.Asn453Ile
XM_011511744.2:c.*48A>T	XP_011510046.1:n.*48A>T
XM_011511750.3:c.1228A>T	XP_011510052.1:p.Thr410Ser
XM_011511756.2:c.863A>T	XP_011510058.1:p.Asn288Ile
XM_024453102.1:c.1208A>T	XP_024308870.1:p.Asn403Ile
XR_001738918.2:n.1690A>T
XR_001738919.2:n.1624A>T
XR_923004.3:n.1947A>T
XR_923007.3:n.1657A>T
XR_923011.3:n.1758A>T
NM_152783.5:c.1316A>T MANE Select	NP_689996.4:p.Asn439Ile
NM_001287249.2:c.914A>T	NP_001274178.1:p.Asn305Ile
NM_001352824.2:c.755A>T	NP_001339753.1:p.Asn252Ile
NR_109778.2:n.1187A>T