Canonical Allele Identifier: CA2764118318

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744895_154744896insACA , CM000666.2:g.154744895_154744896insACA	GRCh38
NC_000004.11:g.155666047_155666048insACA , CM000666.1:g.155666047_155666048insACA	GRCh37
NC_000004.10:g.155885497_155885498insACA	NCBI36
NG_009110.1:g.5885_5886insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.540+29_540+30insACA MANE Select	ENSP00000337224.3:n.540+29_540+30insACA
ENST00000336356.3:c.540+29_540+30insACA	ENSP00000337224.3:n.540+29_540+30insACA
ENST00000499392.1:n.472-3294_472-3293insACA
ENST00000507827.5:c.540+29_540+30insACA	ENSP00000426761.1:n.540+29_540+30insACA
ENST00000510733.1:n.867+29_867+30insACA
NM_001301645.1:c.540+29_540+30insACA	NP_001288574.1:n.540+29_540+30insACA
NM_004744.4:c.540+29_540+30insACA	NP_004735.2:n.540+29_540+30insACA
XM_006714412.2:c.540+29_540+30insACA	XP_006714475.1:n.540+29_540+30insACA
XR_938793.1:n.876+29_876+30insACA
XR_938793.2:n.872+29_872+30insACA
NM_004744.5:c.540+29_540+30insACA MANE Select	NP_004735.2:n.540+29_540+30insACA
NM_001301645.2:c.540+29_540+30insACA	NP_001288574.1:n.540+29_540+30insACA