Canonical Allele Identifier: CA2136124061
Gene: L2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50269167T= , CM000676.2:g.50269167T= GRCh38
NC_000014.8:g.50735885T= , CM000676.1:g.50735885T= GRCh37
NC_000014.7:g.49805635T= NCBI36
NG_008092.1:g.48063A=

Transcript Alleles

HGVS Amino-acid change
ENST00000267436.9:c.902A= MANE Select ENSP00000267436.4:p.Tyr301=
ENST00000261699.8:c.902A= ENSP00000261699.4:p.Tyr301=
ENST00000267436.8:c.902A= ENSP00000267436.4:p.Tyr301=
ENST00000421284.7:c.902A= ENSP00000405559.3:p.Tyr301=
NM_024884.2:c.902A= NP_079160.1:p.Tyr301=
XM_005268075.3:c.902A= XP_005268132.1:p.Tyr301=
XM_011537166.1:c.791A= XP_011535468.1:p.Tyr264=
XM_011537167.1:c.767A= XP_011535469.1:p.Tyr256=
XM_011537168.1:c.356A= XP_011535470.1:p.Tyr119=
XM_011537169.1:c.356A= XP_011535471.1:p.Tyr119=
XM_005268075.5:c.902A= XP_005268132.1:p.Tyr301=
XM_011537166.3:c.791A= XP_011535468.1:p.Tyr264=
XM_011537167.3:c.767A= XP_011535469.1:p.Tyr256=
XM_011537168.3:c.356A= XP_011535470.1:p.Tyr119=
XM_017021655.2:c.791A= XP_016877144.1:p.Tyr264=
XM_017021656.2:c.356A= XP_016877145.1:p.Tyr119=
XM_017021657.2:c.356A= XP_016877146.1:p.Tyr119=
NM_024884.3:c.902A= MANE Select NP_079160.1:p.Tyr301=