Canonical Allele Identifier: CA645540057
Gene: LRAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744844del , CM000666.2:g.154744844del GRCh38
NC_000004.11:g.155665996del , CM000666.1:g.155665996del GRCh37
NC_000004.10:g.155885446del NCBI36
NG_009110.1:g.5834del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.518del MANE Select ENSP00000337224.3:p.Pro173ArgfsTer13
ENST00000336356.3:c.518del ENSP00000337224.3:p.Pro173ArgfsTer13
ENST00000499392.1:n.472-3345del
ENST00000507827.5:c.518del ENSP00000426761.1:p.Pro173ArgfsTer13
ENST00000510733.1:n.845del
NM_001301645.1:c.518del NP_001288574.1:p.Pro173ArgfsTer13
NM_004744.4:c.518del NP_004735.2:p.Pro173ArgfsTer13
XM_006714412.2:c.518del XP_006714475.1:p.Pro173ArgfsTer13
XR_938793.1:n.854del
XR_938793.2:n.850del
NM_004744.5:c.518del MANE Select NP_004735.2:p.Pro173ArgfsTer13
NM_001301645.2:c.518del NP_001288574.1:p.Pro173ArgfsTer13