Canonical Allele Identifier: CA358630571

Gene: LRAT

Linked Data

• ClinVar Variation Id: 1002357
• ClinVar RCV Id: RCV001298772 ; RCV002486147
• dbSNP Id: rs1732845050
• MyVariant Identifiers: chr4:g.155665860G>C (hg19) ; chr4:g.154744708G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744708G>C , CM000666.2:g.154744708G>C	GRCh38
NC_000004.11:g.155665860G>C , CM000666.1:g.155665860G>C	GRCh37
NC_000004.10:g.155885310G>C	NCBI36
NG_009110.1:g.5698G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.382G>C MANE Select	ENSP00000337224.3:p.Asp128His
ENST00000336356.3:c.382G>C	ENSP00000337224.3:p.Asp128His
ENST00000499392.1:n.472-3481G>C
ENST00000507827.5:c.382G>C	ENSP00000426761.1:p.Asp128His
ENST00000510733.1:n.709G>C
NM_001301645.1:c.382G>C	NP_001288574.1:p.Asp128His
NM_004744.4:c.382G>C	NP_004735.2:p.Asp128His
XM_006714412.2:c.382G>C	XP_006714475.1:p.Asp128His
XR_938793.1:n.718G>C
XR_938793.2:n.714G>C
NM_004744.5:c.382G>C MANE Select	NP_004735.2:p.Asp128His
NM_001301645.2:c.382G>C	NP_001288574.1:p.Asp128His