Canonical Allele Identifier: CA10620308

Gene: LRAT

Linked Data

• ClinVar Variation Id: 347874
• ClinVar RCV Id: RCV000271194 ; RCV000328759 ; RCV000386645
• dbSNP Id: rs530211304
• gnomAD v2: 4-155672751-T-C
• gnomAD v3: 4-154751599-T-C
• gnomAD v4: 4-154751599-T-C
• MyVariant Identifiers: chr4:g.155672751T>C (hg19) ; chr4:g.154751599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154751599T>C , CM000666.2:g.154751599T>C	GRCh38
NC_000004.11:g.155672751T>C , CM000666.1:g.155672751T>C	GRCh37
NC_000004.10:g.155892201T>C	NCBI36
NG_009110.1:g.12589T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336356.4:c.*2463T>C MANE Select	ENSP00000337224.3:n.*2463T>C
ENST00000336356.3:c.*2463T>C	ENSP00000337224.3:n.*2463T>C
ENST00000510733.1:n.3483T>C
NM_001301645.1:c.*2463T>C	NP_001288574.1:n.*2463T>C
NM_004744.4:c.*2463T>C	NP_004735.2:n.*2463T>C
NM_004744.5:c.*2463T>C MANE Select	NP_004735.2:n.*2463T>C
NM_001301645.2:c.*2463T>C	NP_001288574.1:n.*2463T>C