Canonical Allele Identifier: CA3115826
Gene: LRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744491G>A , CM000666.2:g.154744491G>A GRCh38
NC_000004.11:g.155665643G>A , CM000666.1:g.155665643G>A GRCh37
NC_000004.10:g.155885093G>A NCBI36
NG_009110.1:g.5481G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.165G>A MANE Select ENSP00000337224.3:p.Arg55=
ENST00000336356.3:c.165G>A ENSP00000337224.3:p.Arg55=
ENST00000499392.1:n.472-3698G>A
ENST00000502525.5:c.165G>A ENSP00000422324.1:p.Arg55=
ENST00000507827.5:c.165G>A ENSP00000426761.1:p.Arg55=
ENST00000510733.1:n.492G>A
NM_001301645.1:c.165G>A NP_001288574.1:p.Arg55=
NM_004744.4:c.165G>A NP_004735.2:p.Arg55=
XM_006714412.2:c.165G>A XP_006714475.1:p.Arg55=
XR_938793.1:n.501G>A
XR_938793.2:n.497G>A
NM_004744.5:c.165G>A MANE Select NP_004735.2:p.Arg55=
NM_001301645.2:c.165G>A NP_001288574.1:p.Arg55=