Canonical Allele Identifier: CA2695203954
Gene: LRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744845del , CM000666.2:g.154744845del GRCh38
NC_000004.11:g.155665997del , CM000666.1:g.155665997del GRCh37
NC_000004.10:g.155885447del NCBI36
NG_009110.1:g.5835del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.519del MANE Select ENSP00000337224.3:p.Ile174SerfsTer12
ENST00000336356.3:c.519del ENSP00000337224.3:p.Ile174SerfsTer12
ENST00000499392.1:n.472-3344del
ENST00000507827.5:c.519del ENSP00000426761.1:p.Ile174SerfsTer12
ENST00000510733.1:n.846del
NM_001301645.1:c.519del NP_001288574.1:p.Ile174SerfsTer12
NM_004744.4:c.519del NP_004735.2:p.Ile174SerfsTer12
XM_006714412.2:c.519del XP_006714475.1:p.Ile174SerfsTer12
XR_938793.1:n.855del
XR_938793.2:n.851del
NM_004744.5:c.519del MANE Select NP_004735.2:p.Ile174SerfsTer12
NM_001301645.2:c.519del NP_001288574.1:p.Ile174SerfsTer12