Canonical Allele Identifier: CA503854839

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49582462C>G , CM000680.2:g.49582462C>G	GRCh38
NC_000018.9:g.47108832C>G , CM000680.1:g.47108832C>G	GRCh37
NC_000018.8:g.45362830C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.1137C>G MANE Select	ENSP00000261292.4:p.Ser379=
ENST00000261292.8:c.1137C>G	ENSP00000261292.4:p.Ser379=
ENST00000427224.6:c.915C>G	ENSP00000387978.2:p.Ser305=
NM_001308006.1:c.915C>G	NP_001294935.1:p.Ser305=
NM_006033.2:c.1137C>G	NP_006024.1:p.Ser379=
NM_006033.3:c.1137C>G	NP_006024.1:p.Ser379=
XM_005258390.1:c.1245C>G	XP_005258447.1:p.Ser415=
XM_011526265.1:c.1023C>G	XP_011524567.1:p.Ser341=
XM_011526267.1:c.897C>G	XP_011524569.1:p.Ser299=
XM_011526265.3:c.1023C>G	XP_011524567.1:p.Ser341=
XM_017026095.1:c.546C>G	XP_016881584.1:p.Ser182=
NM_006033.4:c.1137C>G MANE Select	NP_006024.1:p.Ser379=
NM_001308006.2:c.915C>G	NP_001294935.1:p.Ser305=