Canonical Allele Identifier: CA789407756

Gene: LRAT

Linked Data

• dbSNP Id: rs1337578782
• gnomAD v4: 4-154744892-G-C
• MyVariant Identifiers: chr4:g.155666044G>C (hg19) ; chr4:g.154744892G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744892G>C , CM000666.2:g.154744892G>C	GRCh38
NC_000004.11:g.155666044G>C , CM000666.1:g.155666044G>C	GRCh37
NC_000004.10:g.155885494G>C	NCBI36
NG_009110.1:g.5882G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.540+26G>C MANE Select	ENSP00000337224.3:n.540+26G>C
ENST00000336356.3:c.540+26G>C	ENSP00000337224.3:n.540+26G>C
ENST00000499392.1:n.472-3297G>C
ENST00000507827.5:c.540+26G>C	ENSP00000426761.1:n.540+26G>C
ENST00000510733.1:n.867+26G>C
NM_001301645.1:c.540+26G>C	NP_001288574.1:n.540+26G>C
NM_004744.4:c.540+26G>C	NP_004735.2:n.540+26G>C
XM_006714412.2:c.540+26G>C	XP_006714475.1:n.540+26G>C
XR_938793.1:n.876+26G>C
XR_938793.2:n.872+26G>C
NM_004744.5:c.540+26G>C MANE Select	NP_004735.2:n.540+26G>C
NM_001301645.2:c.540+26G>C	NP_001288574.1:n.540+26G>C