Canonical Allele Identifier: CA9979370

Gene: LIPI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.14144655A= , CM000683.2:g.14144655A=	GRCh38
NG_021434.2:g.67279T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001302998.2:c.1263T= MANE Select	NP_001289927.1:p.Ser421=
ENST00000681601.1:c.1263T= MANE Select	ENSP00000505323.1:p.Ser421=
NM_001302998.1:c.1263T=	NP_001289927.1:p.Ser421=
NM_001302999.1:c.1173T=	NP_001289928.1:p.Ser391=
NM_001302999.2:c.1173T=	NP_001289928.1:p.Ser391=
NM_001303000.1:c.1245T=	NP_001289929.1:p.Ser415=
NM_001303000.2:c.1245T=	NP_001289929.1:p.Ser415=
NM_001303001.1:c.1006+18764T=	NP_001289930.1:n.1006+18764T=
NM_001303001.2:c.1006+18764T=	NP_001289930.1:n.1006+18764T=
NM_001379565.1:c.1158T=	NP_001366494.1:p.Ser386=
NM_001379566.1:c.768T=	NP_001366495.1:p.Ser256=
NM_198996.3:c.1326T=	NP_945347.2:p.Ser442=
NM_198996.4:c.1128T=	NP_945347.3:p.Ser376=
ENST00000344577.6:c.1326T=	ENSP00000343331.2:p.Ser442=
ENST00000400211.3:c.1006+18764T=	ENSP00000383072.3:n.1006+18764T=
ENST00000536861.5:c.1236T=	ENSP00000440381.2:p.Ser412=
ENST00000536861.6:c.1245T=	ENSP00000440381.3:p.Ser415=
ENST00000614229.4:c.1146T=	ENSP00000482652.1:p.Ser382=
ENST00000614229.5:c.1173T=	ENSP00000482652.2:p.Ser391=
ENST00000679868.1:c.768T=	ENSP00000506458.1:p.Ser256=
ENST00000680487.1:c.*267T=	ENSP00000506194.1:n.*267T=
ENST00000680801.1:c.1158T=	ENSP00000505904.1:p.Ser386=
XM_006723966.1:c.1075+18782T=	XP_006724029.1:n.1075+18782T=