Canonical Allele Identifier: CA1505012008

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744851T= , CM000666.2:g.154744851T=	GRCh38
NC_000004.11:g.155666003T= , CM000666.1:g.155666003T=	GRCh37
NC_000004.10:g.155885453T=	NCBI36
NG_009110.1:g.5841T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004744.5:c.525T= MANE Select	NP_004735.2:p.Ser175=
ENST00000336356.4:c.525T= MANE Select	ENSP00000337224.3:p.Ser175=
NM_001301645.1:c.525T=	NP_001288574.1:p.Ser175=
NM_001301645.2:c.525T=	NP_001288574.1:p.Ser175=
NM_004744.4:c.525T=	NP_004735.2:p.Ser175=
ENST00000336356.3:c.525T=	ENSP00000337224.3:p.Ser175=
ENST00000499392.1:n.472-3338T=
ENST00000507827.5:c.525T=	ENSP00000426761.1:p.Ser175=
ENST00000510733.1:n.852T=
XM_006714412.2:c.525T=	XP_006714475.1:p.Ser175=
XR_938793.1:n.861T=
XR_938793.2:n.857T=