Canonical Allele Identifier: CA358630855

Gene: LRAT

Linked Data

• gnomAD v4: 4-154744840-A-G
• MyVariant Identifiers: chr4:g.155665992A>G (hg19) ; chr4:g.154744840A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744840A>G , CM000666.2:g.154744840A>G	GRCh38
NC_000004.11:g.155665992A>G , CM000666.1:g.155665992A>G	GRCh37
NC_000004.10:g.155885442A>G	NCBI36
NG_009110.1:g.5830A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.514A>G MANE Select	ENSP00000337224.3:p.Thr172Ala
ENST00000336356.3:c.514A>G	ENSP00000337224.3:p.Thr172Ala
ENST00000499392.1:n.472-3349A>G
ENST00000507827.5:c.514A>G	ENSP00000426761.1:p.Thr172Ala
ENST00000510733.1:n.841A>G
NM_001301645.1:c.514A>G	NP_001288574.1:p.Thr172Ala
NM_004744.4:c.514A>G	NP_004735.2:p.Thr172Ala
XM_006714412.2:c.514A>G	XP_006714475.1:p.Thr172Ala
XR_938793.1:n.850A>G
XR_938793.2:n.846A>G
NM_004744.5:c.514A>G MANE Select	NP_004735.2:p.Thr172Ala
NM_001301645.2:c.514A>G	NP_001288574.1:p.Thr172Ala