Canonical Allele Identifier: CA358630792

Gene: LRAT

Linked Data

• MyVariant Identifiers: chr4:g.155665964G>C (hg19) ; chr4:g.154744812G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744812G>C , CM000666.2:g.154744812G>C	GRCh38
NC_000004.11:g.155665964G>C , CM000666.1:g.155665964G>C	GRCh37
NC_000004.10:g.155885414G>C	NCBI36
NG_009110.1:g.5802G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.486G>C MANE Select	ENSP00000337224.3:p.Glu162Asp
ENST00000336356.3:c.486G>C	ENSP00000337224.3:p.Glu162Asp
ENST00000499392.1:n.472-3377G>C
ENST00000507827.5:c.486G>C	ENSP00000426761.1:p.Glu162Asp
ENST00000510733.1:n.813G>C
NM_001301645.1:c.486G>C	NP_001288574.1:p.Glu162Asp
NM_004744.4:c.486G>C	NP_004735.2:p.Glu162Asp
XM_006714412.2:c.486G>C	XP_006714475.1:p.Glu162Asp
XR_938793.1:n.822G>C
XR_938793.2:n.818G>C
NM_004744.5:c.486G>C MANE Select	NP_004735.2:p.Glu162Asp
NM_001301645.2:c.486G>C	NP_001288574.1:p.Glu162Asp