Canonical Allele Identifier: CA108930228

Gene: LRAT

Linked Data

• dbSNP Id: rs959565413
• gnomAD v3: 4-154744889-G-A
• gnomAD v4: 4-154744889-G-A
• MyVariant Identifiers: chr4:g.155666041G>A (hg19) ; chr4:g.154744889G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744889G>A , CM000666.2:g.154744889G>A	GRCh38
NC_000004.11:g.155666041G>A , CM000666.1:g.155666041G>A	GRCh37
NC_000004.10:g.155885491G>A	NCBI36
NG_009110.1:g.5879G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.540+23G>A MANE Select	ENSP00000337224.3:n.540+23G>A
ENST00000336356.3:c.540+23G>A	ENSP00000337224.3:n.540+23G>A
ENST00000499392.1:n.472-3300G>A
ENST00000507827.5:c.540+23G>A	ENSP00000426761.1:n.540+23G>A
ENST00000510733.1:n.867+23G>A
NM_001301645.1:c.540+23G>A	NP_001288574.1:n.540+23G>A
NM_004744.4:c.540+23G>A	NP_004735.2:n.540+23G>A
XM_006714412.2:c.540+23G>A	XP_006714475.1:n.540+23G>A
XR_938793.1:n.876+23G>A
XR_938793.2:n.872+23G>A
NM_004744.5:c.540+23G>A MANE Select	NP_004735.2:n.540+23G>A
NM_001301645.2:c.540+23G>A	NP_001288574.1:n.540+23G>A