Canonical Allele Identifier: CA299944078

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49586767C>T , CM000680.2:g.49586767C>T	GRCh38
NC_000018.9:g.47113137C>T , CM000680.1:g.47113137C>T	GRCh37
NC_000018.8:g.45367135C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.1398C>T MANE Select	ENSP00000261292.4:p.Asp466=
ENST00000261292.8:c.1398C>T	ENSP00000261292.4:p.Asp466=
ENST00000427224.6:c.1176C>T	ENSP00000387978.2:p.Asp392=
NM_001308006.1:c.1176C>T	NP_001294935.1:p.Asp392=
NM_006033.2:c.1398C>T	NP_006024.1:p.Asp466=
NM_006033.3:c.1398C>T	NP_006024.1:p.Asp466=
XM_005258390.1:c.1506C>T	XP_005258447.1:p.Asp502=
XM_011526265.1:c.1284C>T	XP_011524567.1:p.Asp428=
XM_011526267.1:c.1158C>T	XP_011524569.1:p.Asp386=
XM_011526265.3:c.1284C>T	XP_011524567.1:p.Asp428=
XM_017026095.1:c.807C>T	XP_016881584.1:p.Asp269=
NM_006033.4:c.1398C>T MANE Select	NP_006024.1:p.Asp466=
NM_001308006.2:c.1176C>T	NP_001294935.1:p.Asp392=