Canonical Allele Identifier: CA2136123969

Gene: L2HGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50268991G= , CM000676.2:g.50268991G=	GRCh38
NC_000014.8:g.50735709G= , CM000676.1:g.50735709G=	GRCh37
NC_000014.7:g.49805459G=	NCBI36
NG_008092.1:g.48239C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267436.9:c.906+172C= MANE Select	ENSP00000267436.4:n.906+172C=
ENST00000261699.8:c.906+172C=	ENSP00000261699.4:n.906+172C=
ENST00000267436.8:c.906+172C=	ENSP00000267436.4:n.906+172C=
ENST00000421284.7:c.906+172C=	ENSP00000405559.3:n.906+172C=
NM_024884.2:c.906+172C=	NP_079160.1:n.906+172C=
XM_005268075.3:c.906+172C=	XP_005268132.1:n.906+172C=
XM_011537166.1:c.795+172C=	XP_011535468.1:n.795+172C=
XM_011537167.1:c.771+172C=	XP_011535469.1:n.771+172C=
XM_011537168.1:c.360+172C=	XP_011535470.1:n.360+172C=
XM_011537169.1:c.360+172C=	XP_011535471.1:n.360+172C=
XM_005268075.5:c.906+172C=	XP_005268132.1:n.906+172C=
XM_011537166.3:c.795+172C=	XP_011535468.1:n.795+172C=
XM_011537167.3:c.771+172C=	XP_011535469.1:n.771+172C=
XM_011537168.3:c.360+172C=	XP_011535470.1:n.360+172C=
XM_017021655.2:c.795+172C=	XP_016877144.1:n.795+172C=
XM_017021656.2:c.360+172C=	XP_016877145.1:n.360+172C=
XM_017021657.2:c.360+172C=	XP_016877146.1:n.360+172C=
NM_024884.3:c.906+172C= MANE Select	NP_079160.1:n.906+172C=