Canonical Allele Identifier: CA1505014755
Gene: LRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154751601_154751602delinsGC , CM000666.2:g.154751601_154751602delinsGC GRCh38
NC_000004.11:g.155672753_155672754delinsGC , CM000666.1:g.155672753_155672754delinsGC GRCh37
NC_000004.10:g.155892203_155892204delinsGC NCBI36
NG_009110.1:g.12591_12592delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.*2465_*2466delinsGC MANE Select ENSP00000337224.3:n.*2465_*2466delinsGC
ENST00000336356.3:c.*2465_*2466delinsGC ENSP00000337224.3:n.*2465_*2466delinsGC
ENST00000510733.1:n.3485_3486delinsGC
NM_001301645.1:c.*2465_*2466delinsGC NP_001288574.1:n.*2465_*2466delinsGC
NM_004744.4:c.*2465_*2466delinsGC NP_004735.2:n.*2465_*2466delinsGC
NM_004744.5:c.*2465_*2466delinsGC MANE Select NP_004735.2:n.*2465_*2466delinsGC
NM_001301645.2:c.*2465_*2466delinsGC NP_001288574.1:n.*2465_*2466delinsGC