Canonical Allele Identifier: CA2764118302

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744874_154744875insACT , CM000666.2:g.154744874_154744875insACT	GRCh38
NC_000004.11:g.155666026_155666027insACT , CM000666.1:g.155666026_155666027insACT	GRCh37
NC_000004.10:g.155885476_155885477insACT	NCBI36
NG_009110.1:g.5864_5865insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.540+8_540+9insACT MANE Select	ENSP00000337224.3:n.540+8_540+9insACT
ENST00000336356.3:c.540+8_540+9insACT	ENSP00000337224.3:n.540+8_540+9insACT
ENST00000499392.1:n.472-3315_472-3314insACT
ENST00000507827.5:c.540+8_540+9insACT	ENSP00000426761.1:n.540+8_540+9insACT
ENST00000510733.1:n.867+8_867+9insACT
NM_001301645.1:c.540+8_540+9insACT	NP_001288574.1:n.540+8_540+9insACT
NM_004744.4:c.540+8_540+9insACT	NP_004735.2:n.540+8_540+9insACT
XM_006714412.2:c.540+8_540+9insACT	XP_006714475.1:n.540+8_540+9insACT
XR_938793.1:n.876+8_876+9insACT
XR_938793.2:n.872+8_872+9insACT
NM_004744.5:c.540+8_540+9insACT MANE Select	NP_004735.2:n.540+8_540+9insACT
NM_001301645.2:c.540+8_540+9insACT	NP_001288574.1:n.540+8_540+9insACT