Canonical Allele Identifier: CA2672449899
Gene: LRAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154751614G>T , CM000666.2:g.154751614G>T GRCh38
NC_000004.11:g.155672766G>T , CM000666.1:g.155672766G>T GRCh37
NC_000004.10:g.155892216G>T NCBI36
NG_009110.1:g.12604G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.*2478G>T MANE Select ENSP00000337224.3:n.*2478G>T
ENST00000336356.3:c.*2478G>T ENSP00000337224.3:n.*2478G>T
ENST00000510733.1:n.3498G>T
NM_001301645.1:c.*2478G>T NP_001288574.1:n.*2478G>T
NM_004744.4:c.*2478G>T NP_004735.2:n.*2478G>T
NM_004744.5:c.*2478G>T MANE Select NP_004735.2:n.*2478G>T
NM_001301645.2:c.*2478G>T NP_001288574.1:n.*2478G>T