Canonical Allele Identifier: CA442020198

Gene: LRAT

Linked Data

• MyVariant Identifiers: chr4:g.155665856C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744704C>T , CM000666.2:g.154744704C>T	GRCh38
NC_000004.11:g.155665856C>T , CM000666.1:g.155665856C>T	GRCh37
NC_000004.10:g.155885306C>T	NCBI36
NG_009110.1:g.5694C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.378C>T MANE Select	ENSP00000337224.3:p.His126=
ENST00000336356.3:c.378C>T	ENSP00000337224.3:p.His126=
ENST00000499392.1:n.472-3485C>T
ENST00000507827.5:c.378C>T	ENSP00000426761.1:p.His126=
ENST00000510733.1:n.705C>T
NM_001301645.1:c.378C>T	NP_001288574.1:p.His126=
NM_004744.4:c.378C>T	NP_004735.2:p.His126=
XM_006714412.2:c.378C>T	XP_006714475.1:p.His126=
XR_938793.1:n.714C>T
XR_938793.2:n.710C>T
NM_004744.5:c.378C>T MANE Select	NP_004735.2:p.His126=
NM_001301645.2:c.378C>T	NP_001288574.1:p.His126=