Canonical Allele Identifier: CA5591956

Gene: LIPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88770903C>A , CM000672.2:g.88770903C>A	GRCh38
NC_000010.10:g.90530660C>A , CM000672.1:g.90530660C>A	GRCh37
NC_000010.9:g.90520640C>A	NCBI36
NG_031911.1:g.14498C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404459.2:c.731C>A MANE Select	ENSP00000383923.1:p.Thr244Asn
ENST00000404459.1:c.731C>A	ENSP00000383923.1:p.Thr244Asn
NM_001102469.1:c.731C>A	NP_001095939.1:p.Thr244Asn
XM_005270049.2:c.731C>A	XP_005270106.1:p.Thr244Asn
XM_011540083.1:c.731C>A	XP_011538385.1:p.Thr244Asn
XM_011540084.1:c.731C>A	XP_011538386.1:p.Thr244Asn
XM_011540085.1:c.731C>A	XP_011538387.1:p.Thr244Asn
XM_011540086.1:c.731C>A	XP_011538388.1:p.Thr244Asn
XR_945801.1:n.1885C>A
XM_005270049.3:c.731C>A	XP_005270106.1:p.Thr244Asn
XM_011540083.2:c.731C>A	XP_011538385.1:p.Thr244Asn
XM_011540084.2:c.731C>A	XP_011538386.1:p.Thr244Asn
XM_011540085.2:c.731C>A	XP_011538387.1:p.Thr244Asn
XM_011540086.2:c.731C>A	XP_011538388.1:p.Thr244Asn
NM_001102469.2:c.731C>A MANE Select	NP_001095939.1:p.Thr244Asn