Canonical Allele Identifier: CA172456

Gene: L2HGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50283947T>C , CM000676.2:g.50283947T>C	GRCh38
NC_000014.8:g.50750665T>C , CM000676.1:g.50750665T>C	GRCh37
NC_000014.7:g.49820415T>C	NCBI36
NG_008092.1:g.33283A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024884.3:c.627A>G MANE Select	NP_079160.1:p.Ala209=
ENST00000267436.9:c.627A>G MANE Select	ENSP00000267436.4:p.Ala209=
NM_024884.2:c.627A>G	NP_079160.1:p.Ala209=
ENST00000261699.8:c.627A>G	ENSP00000261699.4:p.Ala209=
ENST00000267436.8:c.627A>G	ENSP00000267436.4:p.Ala209=
ENST00000421284.7:c.627A>G	ENSP00000405559.3:p.Ala209=
ENST00000555423.5:c.627A>G	ENSP00000450494.1:p.Ala209=
ENST00000555610.1:c.*70A>G	ENSP00000452483.1:n.*70A>G
XM_005268075.3:c.627A>G	XP_005268132.1:p.Ala209=
XM_005268075.5:c.627A>G	XP_005268132.1:p.Ala209=
XM_011537166.1:c.516A>G	XP_011535468.1:p.Ala172=
XM_011537166.3:c.516A>G	XP_011535468.1:p.Ala172=
XM_011537167.1:c.492A>G	XP_011535469.1:p.Ala164=
XM_011537167.3:c.492A>G	XP_011535469.1:p.Ala164=
XM_011537168.1:c.81A>G	XP_011535470.1:p.Ala27=
XM_011537168.3:c.81A>G	XP_011535470.1:p.Ala27=
XM_011537169.1:c.81A>G	XP_011535471.1:p.Ala27=
XM_017021655.2:c.516A>G	XP_016877144.1:p.Ala172=
XM_017021656.2:c.81A>G	XP_016877145.1:p.Ala27=
XM_017021657.2:c.81A>G	XP_016877146.1:p.Ala27=
XM_017021658.1:c.627A>G	XP_016877147.1:p.Ala209=
XR_943538.1:n.866A>G