Canonical Allele Identifier: CA358630555
Gene: LRAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1487229
ClinVar RCV Id: RCV002006307
dbSNP Id: rs1560870996

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744700A>G , CM000666.2:g.154744700A>G GRCh38
NC_000004.11:g.155665852A>G , CM000666.1:g.155665852A>G GRCh37
NC_000004.10:g.155885302A>G NCBI36
NG_009110.1:g.5690A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.374A>G MANE Select ENSP00000337224.3:p.Asn125Ser
ENST00000336356.3:c.374A>G ENSP00000337224.3:p.Asn125Ser
ENST00000499392.1:n.472-3489A>G
ENST00000507827.5:c.374A>G ENSP00000426761.1:p.Asn125Ser
ENST00000510733.1:n.701A>G
NM_001301645.1:c.374A>G NP_001288574.1:p.Asn125Ser
NM_004744.4:c.374A>G NP_004735.2:p.Asn125Ser
XM_006714412.2:c.374A>G XP_006714475.1:p.Asn125Ser
XR_938793.1:n.710A>G
XR_938793.2:n.706A>G
NM_004744.5:c.374A>G MANE Select NP_004735.2:p.Asn125Ser
NM_001301645.2:c.374A>G NP_001288574.1:p.Asn125Ser