Canonical Allele Identifier: CA358630476

Gene: LRAT

Linked Data

• MyVariant Identifiers: chr4:g.155665813C>A (hg19) ; chr4:g.154744661C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744661C>A , CM000666.2:g.154744661C>A	GRCh38
NC_000004.11:g.155665813C>A , CM000666.1:g.155665813C>A	GRCh37
NC_000004.10:g.155885263C>A	NCBI36
NG_009110.1:g.5651C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.335C>A MANE Select	ENSP00000337224.3:p.Thr112Lys
ENST00000336356.3:c.335C>A	ENSP00000337224.3:p.Thr112Lys
ENST00000499392.1:n.472-3528C>A
ENST00000507827.5:c.335C>A	ENSP00000426761.1:p.Thr112Lys
ENST00000510733.1:n.662C>A
NM_001301645.1:c.335C>A	NP_001288574.1:p.Thr112Lys
NM_004744.4:c.335C>A	NP_004735.2:p.Thr112Lys
XM_006714412.2:c.335C>A	XP_006714475.1:p.Thr112Lys
XR_938793.1:n.671C>A
XR_938793.2:n.667C>A
NM_004744.5:c.335C>A MANE Select	NP_004735.2:p.Thr112Lys
NM_001301645.2:c.335C>A	NP_001288574.1:p.Thr112Lys