Canonical Allele Identifier: CA358630017

Gene: LRAT

Linked Data

• ClinVar Variation Id: 2259329
• ClinVar RCV Id: RCV002778098
• MyVariant Identifiers: chr4:g.155665597A>C (hg19) ; chr4:g.154744445A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744445A>C , CM000666.2:g.154744445A>C	GRCh38
NC_000004.11:g.155665597A>C , CM000666.1:g.155665597A>C	GRCh37
NC_000004.10:g.155885047A>C	NCBI36
NG_009110.1:g.5435A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.119A>C MANE Select	ENSP00000337224.3:p.Tyr40Ser
ENST00000336356.3:c.119A>C	ENSP00000337224.3:p.Tyr40Ser
ENST00000499392.1:n.472-3744A>C
ENST00000502525.5:c.119A>C	ENSP00000422324.1:p.Tyr40Ser
ENST00000507827.5:c.119A>C	ENSP00000426761.1:p.Tyr40Ser
ENST00000510733.1:n.446A>C
NM_001301645.1:c.119A>C	NP_001288574.1:p.Tyr40Ser
NM_004744.4:c.119A>C	NP_004735.2:p.Tyr40Ser
XM_006714412.2:c.119A>C	XP_006714475.1:p.Tyr40Ser
XR_938793.1:n.455A>C
XR_938793.2:n.451A>C
NM_004744.5:c.119A>C MANE Select	NP_004735.2:p.Tyr40Ser
NM_001301645.2:c.119A>C	NP_001288574.1:p.Tyr40Ser