Canonical Allele Identifier: CA108930202

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744465C>T , CM000666.2:g.154744465C>T	GRCh38
NC_000004.11:g.155665617C>T , CM000666.1:g.155665617C>T	GRCh37
NC_000004.10:g.155885067C>T	NCBI36
NG_009110.1:g.5455C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004744.5:c.139C>T MANE Select	NP_004735.2:p.Arg47Ter
ENST00000336356.4:c.139C>T MANE Select	ENSP00000337224.3:p.Arg47Ter
NM_001301645.1:c.139C>T	NP_001288574.1:p.Arg47Ter
NM_001301645.2:c.139C>T	NP_001288574.1:p.Arg47Ter
NM_004744.4:c.139C>T	NP_004735.2:p.Arg47Ter
ENST00000336356.3:c.139C>T	ENSP00000337224.3:p.Arg47Ter
ENST00000499392.1:n.472-3724C>T
ENST00000502525.5:c.139C>T	ENSP00000422324.1:p.Arg47Ter
ENST00000507827.5:c.139C>T	ENSP00000426761.1:p.Arg47Ter
ENST00000510733.1:n.466C>T
XM_006714412.2:c.139C>T	XP_006714475.1:p.Arg47Ter
XR_938793.1:n.475C>T
XR_938793.2:n.471C>T