Canonical Allele Identifier: CA1505014759
Gene: LRAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154751604G= , CM000666.2:g.154751604G= GRCh38
NC_000004.11:g.155672756G= , CM000666.1:g.155672756G= GRCh37
NC_000004.10:g.155892206G= NCBI36
NG_009110.1:g.12594G=

Transcript Alleles

HGVS Amino-acid change
ENST00000336356.4:c.*2468G= MANE Select ENSP00000337224.3:n.*2468G=
ENST00000336356.3:c.*2468G= ENSP00000337224.3:n.*2468G=
ENST00000510733.1:n.3488G=
NM_001301645.1:c.*2468G= NP_001288574.1:n.*2468G=
NM_004744.4:c.*2468G= NP_004735.2:n.*2468G=
NM_004744.5:c.*2468G= MANE Select NP_004735.2:n.*2468G=
NM_001301645.2:c.*2468G= NP_001288574.1:n.*2468G=
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