Canonical Allele Identifier: CA10581662
Gene: LRAT HGNC NCBI

Linked Data

ClinVar Variation Id: 236451
ClinVar RCV Id: RCV000225673 RCV000760505
dbSNP Id: rs878853351
MyVariant Identifiers: chr4:g.155665951G>A (hg19) chr4:g.154744799G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744799G>A , CM000666.2:g.154744799G>A GRCh38
NC_000004.11:g.155665951G>A , CM000666.1:g.155665951G>A GRCh37
NC_000004.10:g.155885401G>A NCBI36
NG_009110.1:g.5789G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336356.4:c.473G>A MANE Select ENSP00000337224.3:p.Trp158Ter
ENST00000336356.3:c.473G>A ENSP00000337224.3:p.Trp158Ter
ENST00000499392.1:n.472-3390G>A
ENST00000507827.5:c.473G>A ENSP00000426761.1:p.Trp158Ter
ENST00000510733.1:n.800G>A
NM_001301645.1:c.473G>A NP_001288574.1:p.Trp158Ter
NM_004744.4:c.473G>A NP_004735.2:p.Trp158Ter
XM_006714412.2:c.473G>A XP_006714475.1:p.Trp158Ter
XR_938793.1:n.809G>A
XR_938793.2:n.805G>A
NM_004744.5:c.473G>A MANE Select NP_004735.2:p.Trp158Ter
NM_001301645.2:c.473G>A NP_001288574.1:p.Trp158Ter
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