Canonical Allele Identifier: CA441949378

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744395G>A , CM000666.2:g.154744395G>A	GRCh38
NC_000004.11:g.155665547G>A , CM000666.1:g.155665547G>A	GRCh37
NC_000004.10:g.155884997G>A	NCBI36
NG_009110.1:g.5385G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004744.5:c.69G>A MANE Select	NP_004735.2:p.Thr23=
ENST00000336356.4:c.69G>A MANE Select	ENSP00000337224.3:p.Thr23=
NM_001301645.1:c.69G>A	NP_001288574.1:p.Thr23=
NM_001301645.2:c.69G>A	NP_001288574.1:p.Thr23=
NM_004744.4:c.69G>A	NP_004735.2:p.Thr23=
ENST00000336356.3:c.69G>A	ENSP00000337224.3:p.Thr23=
ENST00000499392.1:n.472-3794G>A
ENST00000502525.5:c.69G>A	ENSP00000422324.1:p.Thr23=
ENST00000507827.5:c.69G>A	ENSP00000426761.1:p.Thr23=
ENST00000510733.1:n.396G>A
XM_006714412.2:c.69G>A	XP_006714475.1:p.Thr23=
XR_938793.1:n.405G>A
XR_938793.2:n.401G>A