Canonical Allele Identifier: CA8959397

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49586795C>T , CM000680.2:g.49586795C>T	GRCh38
NC_000018.9:g.47113165C>T , CM000680.1:g.47113165C>T	GRCh37
NC_000018.8:g.45367163C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.1426C>T MANE Select	ENSP00000261292.4:p.Arg476Trp
ENST00000261292.8:c.1426C>T	ENSP00000261292.4:p.Arg476Trp
ENST00000427224.6:c.1204C>T	ENSP00000387978.2:p.Arg402Trp
NM_001308006.1:c.1204C>T	NP_001294935.1:p.Arg402Trp
NM_006033.2:c.1426C>T	NP_006024.1:p.Arg476Trp
NM_006033.3:c.1426C>T	NP_006024.1:p.Arg476Trp
XM_005258390.1:c.1534C>T	XP_005258447.1:p.Arg512Trp
XM_011526265.1:c.1312C>T	XP_011524567.1:p.Arg438Trp
XM_011526267.1:c.1186C>T	XP_011524569.1:p.Arg396Trp
XM_011526265.3:c.1312C>T	XP_011524567.1:p.Arg438Trp
XM_017026095.1:c.835C>T	XP_016881584.1:p.Arg279Trp
NM_006033.4:c.1426C>T MANE Select	NP_006024.1:p.Arg476Trp
NM_001308006.2:c.1204C>T	NP_001294935.1:p.Arg402Trp