Canonical Allele Identifier: CA1505014758
Gene: LRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154751603_154751604delinsCG , CM000666.2:g.154751603_154751604delinsCG GRCh38
NC_000004.11:g.155672755_155672756delinsCG , CM000666.1:g.155672755_155672756delinsCG GRCh37
NC_000004.10:g.155892205_155892206delinsCG NCBI36
NG_009110.1:g.12593_12594delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.*2467_*2468delinsCG MANE Select ENSP00000337224.3:n.*2467_*2468delinsCG
ENST00000336356.3:c.*2467_*2468delinsCG ENSP00000337224.3:n.*2467_*2468delinsCG
ENST00000510733.1:n.3487_3488delinsCG
NM_001301645.1:c.*2467_*2468delinsCG NP_001288574.1:n.*2467_*2468delinsCG
NM_004744.4:c.*2467_*2468delinsCG NP_004735.2:n.*2467_*2468delinsCG
NM_004744.5:c.*2467_*2468delinsCG MANE Select NP_004735.2:n.*2467_*2468delinsCG
NM_001301645.2:c.*2467_*2468delinsCG NP_001288574.1:n.*2467_*2468delinsCG