Canonical Allele Identifier: CA8958965

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49562371C>T , CM000680.2:g.49562371C>T	GRCh38
NC_000018.9:g.47088741C>T , CM000680.1:g.47088741C>T	GRCh37
NC_000018.8:g.45342739C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.63C>T MANE Select	ENSP00000261292.4:p.Ser21=
ENST00000261292.8:c.63C>T	ENSP00000261292.4:p.Ser21=
ENST00000427224.6:c.63C>T	ENSP00000387978.2:p.Ser21=
ENST00000577628.5:c.205+481C>T	ENSP00000463835.1:n.205+481C>T
ENST00000579750.1:c.27C>T	ENSP00000462480.1:p.Ser9=
ENST00000580036.5:c.63C>T	ENSP00000462420.1:p.Ser21=
ENST00000583083.1:c.-144+911C>T	ENSP00000463077.1:n.-144+911C>T
NM_001308006.1:c.63C>T	NP_001294935.1:p.Ser21=
NM_006033.2:c.63C>T	NP_006024.1:p.Ser21=
NM_006033.3:c.63C>T	NP_006024.1:p.Ser21=
XM_005258390.1:c.205+481C>T	XP_005258447.1:n.205+481C>T
XM_011526265.1:c.205+481C>T	XP_011524567.1:n.205+481C>T
XM_011526267.1:c.-144+911C>T	XP_011524569.1:n.-144+911C>T
XM_011526265.3:c.205+481C>T	XP_011524567.1:n.205+481C>T
XM_017026095.1:c.-607+911C>T	XP_016881584.1:n.-607+911C>T
NM_006033.4:c.63C>T MANE Select	NP_006024.1:p.Ser21=
NM_001308006.2:c.63C>T	NP_001294935.1:p.Ser21=