Canonical Allele Identifier: CA917338479
Gene: LRAT HGNC NCBI

Linked Data

dbSNP Id: rs1560874436
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154751606del , CM000666.2:g.154751606del GRCh38
NC_000004.11:g.155672758del , CM000666.1:g.155672758del GRCh37
NC_000004.10:g.155892208del NCBI36
NG_009110.1:g.12596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.*2470del MANE Select ENSP00000337224.3:n.*2470del
ENST00000336356.3:c.*2470del ENSP00000337224.3:n.*2470del
ENST00000510733.1:n.3490del
NM_001301645.1:c.*2470del NP_001288574.1:n.*2470del
NM_004744.4:c.*2470del NP_004735.2:n.*2470del
NM_004744.5:c.*2470del MANE Select NP_004735.2:n.*2470del
NM_001301645.2:c.*2470del NP_001288574.1:n.*2470del
Search 100 bp 5'
Search 100 bp 3'