Canonical Allele Identifier: CA2672449897
Gene: LRAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154751613A>G , CM000666.2:g.154751613A>G GRCh38
NC_000004.11:g.155672765A>G , CM000666.1:g.155672765A>G GRCh37
NC_000004.10:g.155892215A>G NCBI36
NG_009110.1:g.12603A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.*2477A>G MANE Select ENSP00000337224.3:n.*2477A>G
ENST00000336356.3:c.*2477A>G ENSP00000337224.3:n.*2477A>G
ENST00000510733.1:n.3497A>G
NM_001301645.1:c.*2477A>G NP_001288574.1:n.*2477A>G
NM_004744.4:c.*2477A>G NP_004735.2:n.*2477A>G
NM_004744.5:c.*2477A>G MANE Select NP_004735.2:n.*2477A>G
NM_001301645.2:c.*2477A>G NP_001288574.1:n.*2477A>G