Canonical Allele Identifier: CA358630890

Gene: LRAT

Linked Data

• ClinVar Variation Id: 1473191
• ClinVar RCV Id: RCV001977431
• dbSNP Id: rs2111033342
• MyVariant Identifiers: chr4:g.155666009G>T (hg19) ; chr4:g.154744857G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744857G>T , CM000666.2:g.154744857G>T	GRCh38
NC_000004.11:g.155666009G>T , CM000666.1:g.155666009G>T	GRCh37
NC_000004.10:g.155885459G>T	NCBI36
NG_009110.1:g.5847G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.531G>T MANE Select	ENSP00000337224.3:p.Gln177His
ENST00000336356.3:c.531G>T	ENSP00000337224.3:p.Gln177His
ENST00000499392.1:n.472-3332G>T
ENST00000507827.5:c.531G>T	ENSP00000426761.1:p.Gln177His
ENST00000510733.1:n.858G>T
NM_001301645.1:c.531G>T	NP_001288574.1:p.Gln177His
NM_004744.4:c.531G>T	NP_004735.2:p.Gln177His
XM_006714412.2:c.531G>T	XP_006714475.1:p.Gln177His
XR_938793.1:n.867G>T
XR_938793.2:n.863G>T
NM_004744.5:c.531G>T MANE Select	NP_004735.2:p.Gln177His
NM_001301645.2:c.531G>T	NP_001288574.1:p.Gln177His