Canonical Allele Identifier: CA2377696529

Gene: LIPI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.14109044G= , CM000683.2:g.14109044G=	GRCh38
NC_000021.8:g.15481365G= , CM000683.1:g.15481365G=	GRCh37
NC_000021.7:g.14403236G=	NCBI36
NG_021434.2:g.102890C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001302998.2:c.1332C= MANE Select	NP_001289927.1:p.Asp444=
ENST00000681601.1:c.1332C= MANE Select	ENSP00000505323.1:p.Asp444=
NM_001302998.1:c.1332C=	NP_001289927.1:p.Asp444=
NM_001302999.1:c.1242C=	NP_001289928.1:p.Asp414=
NM_001302999.2:c.1242C=	NP_001289928.1:p.Asp414=
NM_001303000.1:c.1314C=	NP_001289929.1:p.Asp438=
NM_001303000.2:c.1314C=	NP_001289929.1:p.Asp438=
NM_001303001.1:c.1043C=	NP_001289930.1:p.Thr348=
NM_001303001.2:c.1043C=	NP_001289930.1:p.Thr348=
NM_001379565.1:c.1227C=	NP_001366494.1:p.Asp409=
NM_001379566.1:c.837C=	NP_001366495.1:p.Asp279=
NM_198996.3:c.1395C=	NP_945347.2:p.Asp465=
NM_198996.4:c.1197C=	NP_945347.3:p.Asp399=
ENST00000344577.6:c.1395C=	ENSP00000343331.2:p.Asp465=
ENST00000400211.3:c.1043C=	ENSP00000383072.3:p.Thr348=
ENST00000536861.5:c.1305C=	ENSP00000440381.2:p.Asp435=
ENST00000536861.6:c.1314C=	ENSP00000440381.3:p.Asp438=
ENST00000614229.4:c.1215C=	ENSP00000482652.1:p.Asp405=
ENST00000614229.5:c.1242C=	ENSP00000482652.2:p.Asp414=
ENST00000679868.1:c.837C=	ENSP00000506458.1:p.Asp279=
ENST00000680487.1:c.*336C=	ENSP00000506194.1:n.*336C=
ENST00000680801.1:c.1227C=	ENSP00000505904.1:p.Asp409=
XM_006723966.1:c.1112C=	XP_006724029.1:p.Thr371=