Canonical Allele Identifier: CA1505011992

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744815C= , CM000666.2:g.154744815C=	GRCh38
NC_000004.11:g.155665967C= , CM000666.1:g.155665967C=	GRCh37
NC_000004.10:g.155885417C=	NCBI36
NG_009110.1:g.5805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.489C= MANE Select	ENSP00000337224.3:p.His163=
ENST00000336356.3:c.489C=	ENSP00000337224.3:p.His163=
ENST00000499392.1:n.472-3374C=
ENST00000507827.5:c.489C=	ENSP00000426761.1:p.His163=
ENST00000510733.1:n.816C=
NM_001301645.1:c.489C=	NP_001288574.1:p.His163=
NM_004744.4:c.489C=	NP_004735.2:p.His163=
XM_006714412.2:c.489C=	XP_006714475.1:p.His163=
XR_938793.1:n.825C=
XR_938793.2:n.821C=
NM_004744.5:c.489C= MANE Select	NP_004735.2:p.His163=
NM_001301645.2:c.489C=	NP_001288574.1:p.His163=