Canonical Allele Identifier: CA1505012026

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744895G= , CM000666.2:g.154744895G=	GRCh38
NC_000004.11:g.155666047G= , CM000666.1:g.155666047G=	GRCh37
NC_000004.10:g.155885497G=	NCBI36
NG_009110.1:g.5885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.540+29G= MANE Select	ENSP00000337224.3:n.540+29G=
ENST00000336356.3:c.540+29G=	ENSP00000337224.3:n.540+29G=
ENST00000499392.1:n.472-3294G=
ENST00000507827.5:c.540+29G=	ENSP00000426761.1:n.540+29G=
ENST00000510733.1:n.867+29G=
NM_001301645.1:c.540+29G=	NP_001288574.1:n.540+29G=
NM_004744.4:c.540+29G=	NP_004735.2:n.540+29G=
XM_006714412.2:c.540+29G=	XP_006714475.1:n.540+29G=
XR_938793.1:n.876+29G=
XR_938793.2:n.872+29G=
NM_004744.5:c.540+29G= MANE Select	NP_004735.2:n.540+29G=
NM_001301645.2:c.540+29G=	NP_001288574.1:n.540+29G=