Canonical Allele Identifier: CA108930214
Gene: LRAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1065731
ClinVar RCV Id: RCV001376402
dbSNP Id: rs920685564
gnomAD v2: 4-155665794-G-A
gnomAD v3: 4-154744642-G-A
gnomAD v4: 4-154744642-G-A
MyVariant Identifiers: chr4:g.155665794G>A (hg19) chr4:g.154744642G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744642G>A , CM000666.2:g.154744642G>A GRCh38
NC_000004.11:g.155665794G>A , CM000666.1:g.155665794G>A GRCh37
NC_000004.10:g.155885244G>A NCBI36
NG_009110.1:g.5632G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.316G>A MANE Select ENSP00000337224.3:p.Ala106Thr
ENST00000336356.3:c.316G>A ENSP00000337224.3:p.Ala106Thr
ENST00000499392.1:n.472-3547G>A
ENST00000507827.5:c.316G>A ENSP00000426761.1:p.Ala106Thr
ENST00000510733.1:n.643G>A
NM_001301645.1:c.316G>A NP_001288574.1:p.Ala106Thr
NM_004744.4:c.316G>A NP_004735.2:p.Ala106Thr
XM_006714412.2:c.316G>A XP_006714475.1:p.Ala106Thr
XR_938793.1:n.652G>A
XR_938793.2:n.648G>A
NM_004744.5:c.316G>A MANE Select NP_004735.2:p.Ala106Thr
NM_001301645.2:c.316G>A NP_001288574.1:p.Ala106Thr
Search 100 bp 5'
Search 100 bp 3'