Canonical Allele Identifier: CA2136124015
Gene: L2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50269083C= , CM000676.2:g.50269083C= GRCh38
NC_000014.8:g.50735801C= , CM000676.1:g.50735801C= GRCh37
NC_000014.7:g.49805551C= NCBI36
NG_008092.1:g.48147G=

Transcript Alleles

HGVS Amino-acid change
ENST00000267436.9:c.906+80G= MANE Select ENSP00000267436.4:n.906+80G=
ENST00000261699.8:c.906+80G= ENSP00000261699.4:n.906+80G=
ENST00000267436.8:c.906+80G= ENSP00000267436.4:n.906+80G=
ENST00000421284.7:c.906+80G= ENSP00000405559.3:n.906+80G=
NM_024884.2:c.906+80G= NP_079160.1:n.906+80G=
XM_005268075.3:c.906+80G= XP_005268132.1:n.906+80G=
XM_011537166.1:c.795+80G= XP_011535468.1:n.795+80G=
XM_011537167.1:c.771+80G= XP_011535469.1:n.771+80G=
XM_011537168.1:c.360+80G= XP_011535470.1:n.360+80G=
XM_011537169.1:c.360+80G= XP_011535471.1:n.360+80G=
XM_005268075.5:c.906+80G= XP_005268132.1:n.906+80G=
XM_011537166.3:c.795+80G= XP_011535468.1:n.795+80G=
XM_011537167.3:c.771+80G= XP_011535469.1:n.771+80G=
XM_011537168.3:c.360+80G= XP_011535470.1:n.360+80G=
XM_017021655.2:c.795+80G= XP_016877144.1:n.795+80G=
XM_017021656.2:c.360+80G= XP_016877145.1:n.360+80G=
XM_017021657.2:c.360+80G= XP_016877146.1:n.360+80G=
NM_024884.3:c.906+80G= MANE Select NP_079160.1:n.906+80G=