Canonical Allele Identifier: CA1069739494

Gene: LRAT

Linked Data

• dbSNP Id: rs1732993804
• gnomAD v3: 4-154751617-C-G
• gnomAD v4: 4-154751617-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154751617C>G , CM000666.2:g.154751617C>G	GRCh38
NC_000004.11:g.155672769C>G , CM000666.1:g.155672769C>G	GRCh37
NC_000004.10:g.155892219C>G	NCBI36
NG_009110.1:g.12607C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.*2481C>G MANE Select	ENSP00000337224.3:n.*2481C>G
ENST00000336356.3:c.*2481C>G	ENSP00000337224.3:n.*2481C>G
ENST00000510733.1:n.3501C>G
NM_001301645.1:c.*2481C>G	NP_001288574.1:n.*2481C>G
NM_004744.4:c.*2481C>G	NP_004735.2:n.*2481C>G
NM_004744.5:c.*2481C>G MANE Select	NP_004735.2:n.*2481C>G
NM_001301645.2:c.*2481C>G	NP_001288574.1:n.*2481C>G