Canonical Allele Identifier: CA10617244
Community Standard Title: NM_004744.5(LRAT):c.258G>A (p.Gly86=)
Gene: LRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744584G>A , CM000666.2:g.154744584G>A GRCh38
NC_000004.11:g.155665736G>A , CM000666.1:g.155665736G>A GRCh37
NC_000004.10:g.155885186G>A NCBI36
NG_009110.1:g.5574G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004744.5:c.258G>A MANE Select NP_004735.2:p.Gly86=
ENST00000336356.4:c.258G>A MANE Select ENSP00000337224.3:p.Gly86=
NM_001301645.1:c.258G>A NP_001288574.1:p.Gly86=
NM_001301645.2:c.258G>A NP_001288574.1:p.Gly86=
NM_004744.4:c.258G>A NP_004735.2:p.Gly86=
ENST00000336356.3:c.258G>A ENSP00000337224.3:p.Gly86=
ENST00000499392.1:n.472-3605G>A
ENST00000507827.5:c.258G>A ENSP00000426761.1:p.Gly86=
ENST00000510733.1:n.585G>A
XM_006714412.2:c.258G>A XP_006714475.1:p.Gly86=
XR_938793.1:n.594G>A
XR_938793.2:n.590G>A