Canonical Allele Identifier: CA1505011989

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744809C= , CM000666.2:g.154744809C=	GRCh38
NC_000004.11:g.155665961C= , CM000666.1:g.155665961C=	GRCh37
NC_000004.10:g.155885411C=	NCBI36
NG_009110.1:g.5799C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.483C= MANE Select	ENSP00000337224.3:p.Cys161=
ENST00000336356.3:c.483C=	ENSP00000337224.3:p.Cys161=
ENST00000499392.1:n.472-3380C=
ENST00000507827.5:c.483C=	ENSP00000426761.1:p.Cys161=
ENST00000510733.1:n.810C=
NM_001301645.1:c.483C=	NP_001288574.1:p.Cys161=
NM_004744.4:c.483C=	NP_004735.2:p.Cys161=
XM_006714412.2:c.483C=	XP_006714475.1:p.Cys161=
XR_938793.1:n.819C=
XR_938793.2:n.815C=
NM_004744.5:c.483C= MANE Select	NP_004735.2:p.Cys161=
NM_001301645.2:c.483C=	NP_001288574.1:p.Cys161=