Canonical Allele Identifier: CA345857881

Gene: LPIN1

Linked Data

• gnomAD v4: 2-11787139-C-G
• MyVariant Identifiers: chr2:g.11927265C>G (hg19) ; chr2:g.11787139C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11787139C>G , CM000664.2:g.11787139C>G	GRCh38
NC_000002.11:g.11927265C>G , CM000664.1:g.11927265C>G	GRCh37
NC_000002.10:g.11844716C>G	NCBI36
NG_012843.2:g.114561C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674199.1:c.1615C>G MANE Select	ENSP00000501331.1:p.Pro539Ala
ENST00000256720.6:c.1507C>G	ENSP00000256720.2:p.Pro503Ala
ENST00000396097.5:c.1633C>G	ENSP00000379404.2:p.Pro545Ala
ENST00000396099.5:c.1633C>G	ENSP00000379406.2:p.Pro545Ala
ENST00000404113.6:n.1100C>G
ENST00000425416.6:c.1525C>G	ENSP00000401522.2:p.Pro509Ala
ENST00000449576.6:c.1762C>G	ENSP00000397908.2:p.Pro588Ala
ENST00000454151.2:c.10C>G	ENSP00000413714.1:p.Pro4Ala
ENST00000464953.2:n.93C>G
NM_001261427.1:c.1525C>G	NP_001248356.1:p.Pro509Ala
NM_001261428.1:c.1762C>G	NP_001248357.1:p.Pro588Ala
NM_145693.2:c.1507C>G	NP_663731.1:p.Pro503Ala
XM_006711869.1:c.1654C>G	XP_006711932.1:p.Pro552Ala
XM_006711870.2:c.1633C>G	XP_006711933.1:p.Pro545Ala
XM_006711871.1:c.1615C>G	XP_006711934.1:p.Pro539Ala
XM_006711872.1:c.1615C>G	XP_006711935.1:p.Pro539Ala
XM_006711874.1:c.1615C>G	XP_006711937.1:p.Pro539Ala
XM_011510333.1:c.1759C>G	XP_011508635.1:p.Pro587Ala
XM_011510334.1:c.1633C>G	XP_011508636.1:p.Pro545Ala
XM_011510335.1:c.1615C>G	XP_011508637.1:p.Pro539Ala
XM_011510336.1:c.1615C>G	XP_011508638.1:p.Pro539Ala
XM_011510337.1:c.1762C>G	XP_011508639.1:p.Pro588Ala
NM_001261427.2:c.1525C>G	NP_001248356.1:p.Pro509Ala
NM_001261428.2:c.1762C>G	NP_001248357.1:p.Pro588Ala
NM_001349199.1:c.1507C>G	NP_001336128.1:p.Pro503Ala
NM_001349200.1:c.1507C>G	NP_001336129.1:p.Pro503Ala
NM_001349201.1:c.1507C>G	NP_001336130.1:p.Pro503Ala
NM_001349202.1:c.1612C>G	NP_001336131.1:p.Pro538Ala
NM_001349203.1:c.1612C>G	NP_001336132.1:p.Pro538Ala
NM_001349204.1:c.1615C>G	NP_001336133.1:p.Pro539Ala
NM_001349205.1:c.1615C>G	NP_001336134.1:p.Pro539Ala
NM_001349206.1:c.1615C>G	NP_001336135.1:p.Pro539Ala
NM_001349207.1:c.1705C>G	NP_001336136.1:p.Pro569Ala
NM_001349208.1:c.1654C>G	NP_001336137.1:p.Pro552Ala
NM_145693.3:c.1507C>G	NP_663731.1:p.Pro503Ala
NR_146080.1:n.1603C>G
XM_006711870.4:c.1633C>G	XP_006711933.1:p.Pro545Ala
XM_006711872.3:c.1615C>G	XP_006711935.1:p.Pro539Ala
XM_011510333.2:c.1759C>G	XP_011508635.1:p.Pro587Ala
XM_011510334.3:c.1633C>G	XP_011508636.1:p.Pro545Ala
XM_011510335.3:c.1615C>G	XP_011508637.1:p.Pro539Ala
XM_011510336.3:c.1615C>G	XP_011508638.1:p.Pro539Ala
XM_017003623.2:c.1684C>G	XP_016859112.1:p.Pro562Ala
XM_017003624.2:c.1615C>G	XP_016859113.1:p.Pro539Ala
XM_017003625.2:c.1615C>G	XP_016859114.1:p.Pro539Ala
XM_017003627.2:c.1612C>G	XP_016859116.1:p.Pro538Ala
XM_017003628.2:c.1507C>G	XP_016859117.1:p.Pro503Ala
XM_017003629.1:c.1507C>G	XP_016859118.1:p.Pro503Ala
XM_017003630.2:c.1507C>G	XP_016859119.1:p.Pro503Ala
XM_024452762.1:c.1615C>G	XP_024308530.1:p.Pro539Ala
XM_024452763.1:c.1525C>G	XP_024308531.1:p.Pro509Ala
NM_001261428.3:c.1762C>G	NP_001248357.1:p.Pro588Ala
NM_001349199.2:c.1507C>G	NP_001336128.1:p.Pro503Ala
NM_001349200.2:c.1507C>G	NP_001336129.1:p.Pro503Ala
NM_001349201.2:c.1507C>G	NP_001336130.1:p.Pro503Ala
NM_001349202.2:c.1612C>G	NP_001336131.1:p.Pro538Ala
NM_001349203.2:c.1612C>G	NP_001336132.1:p.Pro538Ala
NM_001349204.2:c.1615C>G	NP_001336133.1:p.Pro539Ala
NM_001349206.2:c.1615C>G MANE Select	NP_001336135.1:p.Pro539Ala
NM_001349207.2:c.1705C>G	NP_001336136.1:p.Pro569Ala
NM_001349208.2:c.1654C>G	NP_001336137.1:p.Pro552Ala
NM_145693.4:c.1507C>G	NP_663731.1:p.Pro503Ala
NR_146080.2:n.1556C>G
NM_001261427.3:c.1525C>G	NP_001248356.1:p.Pro509Ala
NM_001349205.2:c.1615C>G	NP_001336134.1:p.Pro539Ala