Canonical Allele Identifier: CA1505014765
Gene: LRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154751610_154751613delinsTGTA , CM000666.2:g.154751610_154751613delinsTGTA GRCh38
NC_000004.11:g.155672762_155672765delinsTGTA , CM000666.1:g.155672762_155672765delinsTGTA GRCh37
NC_000004.10:g.155892212_155892215delinsTGTA NCBI36
NG_009110.1:g.12600_12603delinsTGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.*2474_*2477delinsTGTA MANE Select ENSP00000337224.3:n.*2474_*2477delinsTGTA
ENST00000336356.3:c.*2474_*2477delinsTGTA ENSP00000337224.3:n.*2474_*2477delinsTGTA
ENST00000510733.1:n.3494_3497delinsTGTA
NM_001301645.1:c.*2474_*2477delinsTGTA NP_001288574.1:n.*2474_*2477delinsTGTA
NM_004744.4:c.*2474_*2477delinsTGTA NP_004735.2:n.*2474_*2477delinsTGTA
NM_004744.5:c.*2474_*2477delinsTGTA MANE Select NP_004735.2:n.*2474_*2477delinsTGTA
NM_001301645.2:c.*2474_*2477delinsTGTA NP_001288574.1:n.*2474_*2477delinsTGTA