Canonical Allele Identifier: CA358630779

Gene: LRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744807T>C , CM000666.2:g.154744807T>C	GRCh38
NC_000004.11:g.155665959T>C , CM000666.1:g.155665959T>C	GRCh37
NC_000004.10:g.155885409T>C	NCBI36
NG_009110.1:g.5797T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004744.5:c.481T>C MANE Select	NP_004735.2:p.Cys161Arg
ENST00000336356.4:c.481T>C MANE Select	ENSP00000337224.3:p.Cys161Arg
NM_001301645.1:c.481T>C	NP_001288574.1:p.Cys161Arg
NM_001301645.2:c.481T>C	NP_001288574.1:p.Cys161Arg
NM_004744.4:c.481T>C	NP_004735.2:p.Cys161Arg
ENST00000336356.3:c.481T>C	ENSP00000337224.3:p.Cys161Arg
ENST00000499392.1:n.472-3382T>C
ENST00000507827.5:c.481T>C	ENSP00000426761.1:p.Cys161Arg
ENST00000510733.1:n.808T>C
XM_006714412.2:c.481T>C	XP_006714475.1:p.Cys161Arg
XR_938793.1:n.817T>C
XR_938793.2:n.813T>C