Canonical Allele Identifier: CA2136137251

Gene: L2HGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50302132T= , CM000676.2:g.50302132T=	GRCh38
NC_000014.8:g.50768850T= , CM000676.1:g.50768850T=	GRCh37
NC_000014.7:g.49838600T=	NCBI36
NG_008092.1:g.15098A=

Transcript Alleles

HGVS	Amino-acid Change
NM_024884.3:c.293A= MANE Select	NP_079160.1:p.His98=
ENST00000267436.9:c.293A= MANE Select	ENSP00000267436.4:p.His98=
NM_024884.2:c.293A=	NP_079160.1:p.His98=
ENST00000261699.8:c.293A=	ENSP00000261699.4:p.His98=
ENST00000267436.8:c.293A=	ENSP00000267436.4:p.His98=
ENST00000421284.7:c.293A=	ENSP00000405559.3:p.His98=
ENST00000554191.5:c.*156A=	ENSP00000451194.1:n.*156A=
ENST00000555423.5:c.293A=	ENSP00000450494.1:p.His98=
ENST00000555610.1:c.293A=	ENSP00000452483.1:p.His98=
ENST00000556393.1:n.433A=
XM_005268075.3:c.293A=	XP_005268132.1:p.His98=
XM_005268075.5:c.293A=	XP_005268132.1:p.His98=
XM_011537166.1:c.182A=	XP_011535468.1:p.His61=
XM_011537166.3:c.182A=	XP_011535468.1:p.His61=
XM_011537167.1:c.158A=	XP_011535469.1:p.His53=
XM_011537167.3:c.158A=	XP_011535469.1:p.His53=
XM_017021655.2:c.182A=	XP_016877144.1:p.His61=
XM_017021656.2:c.-333A=	XP_016877145.1:n.-333A=
XM_017021657.2:c.-333A=	XP_016877146.1:n.-333A=
XM_017021658.1:c.293A=	XP_016877147.1:p.His98=
XR_943538.1:n.532A=