Canonical Allele Identifier: CA1505012499

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154745783T= , CM000666.2:g.154745783T=	GRCh38
NC_000004.11:g.155666935T= , CM000666.1:g.155666935T=	GRCh37
NC_000004.10:g.155886385T=	NCBI36
NG_009110.1:g.6773T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.540+917T= MANE Select	ENSP00000337224.3:n.540+917T=
ENST00000336356.3:c.540+917T=	ENSP00000337224.3:n.540+917T=
ENST00000499392.1:n.472-2406T=
ENST00000502474.5:n.135+275T=
ENST00000507827.5:c.540+917T=	ENSP00000426761.1:n.540+917T=
ENST00000510733.1:n.867+917T=
ENST00000510919.1:n.96+241T=
NM_001301645.1:c.540+917T=	NP_001288574.1:n.540+917T=
NM_004744.4:c.540+917T=	NP_004735.2:n.540+917T=
XM_006714412.2:c.540+917T=	XP_006714475.1:n.540+917T=
XR_938793.1:n.876+917T=
XR_938793.2:n.872+917T=
NM_004744.5:c.540+917T= MANE Select	NP_004735.2:n.540+917T=
NM_001301645.2:c.540+917T=	NP_001288574.1:n.540+917T=