Canonical Allele Identifier: CA470723762

Gene: LIPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88774487G>A , CM000672.2:g.88774487G>A	GRCh38
NC_000010.10:g.90534244G>A , CM000672.1:g.90534244G>A	GRCh37
NC_000010.9:g.90524224G>A	NCBI36
NG_031911.1:g.18082G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404459.2:c.834G>A MANE Select	ENSP00000383923.1:p.Val278=
ENST00000404459.1:c.834G>A	ENSP00000383923.1:p.Val278=
NM_001102469.1:c.834G>A	NP_001095939.1:p.Val278=
XM_005270049.2:c.834G>A	XP_005270106.1:p.Val278=
XM_011540083.1:c.834G>A	XP_011538385.1:p.Val278=
XM_011540084.1:c.834G>A	XP_011538386.1:p.Val278=
XM_011540085.1:c.820-605G>A	XP_011538387.1:n.820-605G>A
XM_011540086.1:c.819+3496G>A	XP_011538388.1:n.819+3496G>A
XM_005270049.3:c.834G>A	XP_005270106.1:p.Val278=
XM_011540083.2:c.834G>A	XP_011538385.1:p.Val278=
XM_011540084.2:c.834G>A	XP_011538386.1:p.Val278=
XM_011540085.2:c.820-605G>A	XP_011538387.1:n.820-605G>A
XM_011540086.2:c.819+3496G>A	XP_011538388.1:n.819+3496G>A
NM_001102469.2:c.834G>A MANE Select	NP_001095939.1:p.Val278=