Canonical Allele Identifier: CA511421600

Gene: LIPI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.14109008T>G , CM000683.2:g.14109008T>G	GRCh38
NC_000021.8:g.15481329T>G , CM000683.1:g.15481329T>G	GRCh37
NC_000021.7:g.14403200T>G	NCBI36
NG_021434.2:g.102926A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001302998.2:c.1368A>C MANE Select	NP_001289927.1:p.Thr456=
ENST00000681601.1:c.1368A>C MANE Select	ENSP00000505323.1:p.Thr456=
NM_001302998.1:c.1368A>C	NP_001289927.1:p.Thr456=
NM_001302999.1:c.1278A>C	NP_001289928.1:p.Thr426=
NM_001302999.2:c.1278A>C	NP_001289928.1:p.Thr426=
NM_001303000.1:c.1350A>C	NP_001289929.1:p.Thr450=
NM_001303000.2:c.1350A>C	NP_001289929.1:p.Thr450=
NM_001303001.1:c.1079A>C	NP_001289930.1:p.His360Pro
NM_001303001.2:c.1079A>C	NP_001289930.1:p.His360Pro
NM_001379565.1:c.1263A>C	NP_001366494.1:p.Thr421=
NM_001379566.1:c.873A>C	NP_001366495.1:p.Thr291=
NM_198996.3:c.1431A>C	NP_945347.2:p.Thr477=
NM_198996.4:c.1233A>C	NP_945347.3:p.Thr411=
ENST00000344577.6:c.1431A>C	ENSP00000343331.2:p.Thr477=
ENST00000400211.3:c.1079A>C	ENSP00000383072.3:p.His360Pro
ENST00000536861.5:c.1341A>C	ENSP00000440381.2:p.Thr447=
ENST00000536861.6:c.1350A>C	ENSP00000440381.3:p.Thr450=
ENST00000614229.4:c.1251A>C	ENSP00000482652.1:p.Thr417=
ENST00000614229.5:c.1278A>C	ENSP00000482652.2:p.Thr426=
ENST00000679868.1:c.873A>C	ENSP00000506458.1:p.Thr291=
ENST00000680487.1:c.*372A>C	ENSP00000506194.1:n.*372A>C
ENST00000680801.1:c.1263A>C	ENSP00000505904.1:p.Thr421=
XM_006723966.1:c.1148A>C	XP_006724029.1:p.His383Pro