Canonical Allele Identifier: CA358630798

Gene: LRAT

Linked Data

• gnomAD v4: 4-154744815-C-A
• MyVariant Identifiers: chr4:g.155665967C>A (hg19) ; chr4:g.154744815C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744815C>A , CM000666.2:g.154744815C>A	GRCh38
NC_000004.11:g.155665967C>A , CM000666.1:g.155665967C>A	GRCh37
NC_000004.10:g.155885417C>A	NCBI36
NG_009110.1:g.5805C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.489C>A MANE Select	ENSP00000337224.3:p.His163Gln
ENST00000336356.3:c.489C>A	ENSP00000337224.3:p.His163Gln
ENST00000499392.1:n.472-3374C>A
ENST00000507827.5:c.489C>A	ENSP00000426761.1:p.His163Gln
ENST00000510733.1:n.816C>A
NM_001301645.1:c.489C>A	NP_001288574.1:p.His163Gln
NM_004744.4:c.489C>A	NP_004735.2:p.His163Gln
XM_006714412.2:c.489C>A	XP_006714475.1:p.His163Gln
XR_938793.1:n.825C>A
XR_938793.2:n.821C>A
NM_004744.5:c.489C>A MANE Select	NP_004735.2:p.His163Gln
NM_001301645.2:c.489C>A	NP_001288574.1:p.His163Gln