Canonical Allele Identifier: CA555973799

Gene: LRAT

Linked Data

• ClinVar Variation Id: 1494001
• ClinVar RCV Id: RCV002012786
• dbSNP Id: rs1169173848
• gnomAD v2: 4-155665779-GTTA-G
• gnomAD v4: 4-154744627-GTTA-G
• MyVariant Identifiers: chr4:g.155665780_155665782del (hg19) ; chr4:g.154744628_154744630del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744630_154744632del , CM000666.2:g.154744630_154744632del	GRCh38
NC_000004.11:g.155665782_155665784del , CM000666.1:g.155665782_155665784del	GRCh37
NC_000004.10:g.155885232_155885234del	NCBI36
NG_009110.1:g.5620_5622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.304_306del MANE Select	ENSP00000337224.3:p.Ile102del
ENST00000336356.3:c.304_306del	ENSP00000337224.3:p.Ile102del
ENST00000499392.1:n.472-3559_472-3557del
ENST00000507827.5:c.304_306del	ENSP00000426761.1:p.Ile102del
ENST00000510733.1:n.631_633del
NM_001301645.1:c.304_306del	NP_001288574.1:p.Ile102del
NM_004744.4:c.304_306del	NP_004735.2:p.Ile102del
XM_006714412.2:c.304_306del	XP_006714475.1:p.Ile102del
XR_938793.1:n.640_642del
XR_938793.2:n.636_638del
NM_004744.5:c.304_306del MANE Select	NP_004735.2:p.Ile102del
NM_001301645.2:c.304_306del	NP_001288574.1:p.Ile102del