Canonical Allele Identifier: CA10620268

Gene: LRAT

Linked Data

• ClinVar Variation Id: 347846
• ClinVar RCV Id: RCV000268041 ; RCV000307915 ; RCV000362672
• dbSNP Id: rs886059160
• gnomAD v2: 4-155665292-C-T
• gnomAD v3: 4-154744140-C-T
• gnomAD v4: 4-154744140-C-T
• MyVariant Identifiers: chr4:g.155665292C>T (hg19) ; chr4:g.154744140C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744140C>T , CM000666.2:g.154744140C>T	GRCh38
NC_000004.11:g.155665292C>T , CM000666.1:g.155665292C>T	GRCh37
NC_000004.10:g.155884742C>T	NCBI36
NG_009110.1:g.5130C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.-84C>T MANE Select	ENSP00000337224.3:n.-84C>T
ENST00000336356.3:c.-84C>T	ENSP00000337224.3:n.-84C>T
ENST00000499392.1:n.472-4049C>T
ENST00000502525.5:c.-1-186C>T	ENSP00000422324.1:n.-1-186C>T
ENST00000507827.5:c.-1-186C>T	ENSP00000426761.1:n.-1-186C>T
ENST00000510733.1:n.141C>T
NM_001301645.1:c.-1-186C>T	NP_001288574.1:n.-1-186C>T
NM_004744.4:c.-84C>T	NP_004735.2:n.-84C>T
XM_006714412.2:c.-1-186C>T	XP_006714475.1:n.-1-186C>T
XR_938793.1:n.150C>T
XR_938793.2:n.146C>T
NM_004744.5:c.-84C>T MANE Select	NP_004735.2:n.-84C>T
NM_001301645.2:c.-1-186C>T	NP_001288574.1:n.-1-186C>T