Canonical Allele Identifier: CA9979566

Gene: LIPI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.14166356G>C , CM000683.2:g.14166356G>C	GRCh38
NC_000021.8:g.15538677G>C , CM000683.1:g.15538677G>C	GRCh37
NC_000021.7:g.14460548G>C	NCBI36
NG_021434.2:g.45578C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400211.3:c.733+6C>G	ENSP00000383072.3:n.733+6C>G
ENST00000536861.6:c.733+6C>G	ENSP00000440381.3:n.733+6C>G
ENST00000614229.5:c.644-966C>G	ENSP00000482652.2:n.644-966C>G
ENST00000679868.1:c.238+6C>G	ENSP00000506458.1:n.238+6C>G
ENST00000680487.1:c.733+6C>G	ENSP00000506194.1:n.733+6C>G
ENST00000680801.1:c.733+6C>G	ENSP00000505904.1:n.733+6C>G
ENST00000681601.1:c.733+6C>G MANE Select	ENSP00000505323.1:n.733+6C>G
ENST00000344577.6:c.796+6C>G	ENSP00000343331.2:n.796+6C>G
ENST00000400211.2:c.282-966C>G
ENST00000536861.5:c.706+6C>G	ENSP00000440381.2:n.706+6C>G
ENST00000614229.4:c.617-966C>G	ENSP00000482652.1:n.617-966C>G
NM_001302998.1:c.733+6C>G	NP_001289927.1:n.733+6C>G
NM_001302999.1:c.644-966C>G	NP_001289928.1:n.644-966C>G
NM_001303000.1:c.733+6C>G	NP_001289929.1:n.733+6C>G
NM_001303001.1:c.733+6C>G	NP_001289930.1:n.733+6C>G
NM_198996.3:c.796+6C>G	NP_945347.2:n.796+6C>G
XM_006723965.2:c.820+6C>G	XP_006724028.1:n.820+6C>G
XM_006723966.1:c.820+6C>G	XP_006724029.1:n.820+6C>G
XM_006723965.3:c.820+6C>G	XP_006724028.1:n.820+6C>G
NM_001302998.2:c.733+6C>G MANE Select	NP_001289927.1:n.733+6C>G
NM_001302999.2:c.644-966C>G	NP_001289928.1:n.644-966C>G
NM_001303000.2:c.733+6C>G	NP_001289929.1:n.733+6C>G
NM_001303001.2:c.733+6C>G	NP_001289930.1:n.733+6C>G
NM_001379565.1:c.733+6C>G	NP_001366494.1:n.733+6C>G
NM_001379566.1:c.238+6C>G	NP_001366495.1:n.238+6C>G
NM_198996.4:c.598+6C>G	NP_945347.3:n.598+6C>G