Canonical Allele Identifier: CA8959330

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49583568C>T , CM000680.2:g.49583568C>T	GRCh38
NC_000018.9:g.47109938C>T , CM000680.1:g.47109938C>T	GRCh37
NC_000018.8:g.45363936C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.1170C>T MANE Select	ENSP00000261292.4:p.Ile390=
ENST00000261292.8:c.1170C>T	ENSP00000261292.4:p.Ile390=
ENST00000427224.6:c.948C>T	ENSP00000387978.2:p.Ile316=
NM_001308006.1:c.948C>T	NP_001294935.1:p.Ile316=
NM_006033.2:c.1170C>T	NP_006024.1:p.Ile390=
NM_006033.3:c.1170C>T	NP_006024.1:p.Ile390=
XM_005258390.1:c.1278C>T	XP_005258447.1:p.Ile426=
XM_011526265.1:c.1056C>T	XP_011524567.1:p.Ile352=
XM_011526267.1:c.930C>T	XP_011524569.1:p.Ile310=
XM_011526265.3:c.1056C>T	XP_011524567.1:p.Ile352=
XM_017026095.1:c.579C>T	XP_016881584.1:p.Ile193=
NM_006033.4:c.1170C>T MANE Select	NP_006024.1:p.Ile390=
NM_001308006.2:c.948C>T	NP_001294935.1:p.Ile316=