Canonical Allele Identifier: CA2842323629

Gene: LPIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11750266G>A , CM000664.2:g.11750266G>A	GRCh38
NC_000002.11:g.11890392G>A , CM000664.1:g.11890392G>A	GRCh37
NC_000002.10:g.11807843G>A	NCBI36
NG_012843.2:g.77688G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674199.1:c.-10+3595G>A MANE Select	ENSP00000501331.1:n.-10+3595G>A
ENST00000256720.6:c.-10+3595G>A	ENSP00000256720.2:n.-10+3595G>A
ENST00000396097.5:c.9+8838G>A	ENSP00000379404.2:n.9+8838G>A
ENST00000396098.5:c.9+8838G>A	ENSP00000379405.1:n.9+8838G>A
ENST00000396099.5:c.9+8838G>A	ENSP00000379406.2:n.9+8838G>A
ENST00000423495.1:c.-360+3595G>A	ENSP00000392424.1:n.-360+3595G>A
ENST00000425416.6:c.9+8838G>A	ENSP00000401522.2:n.9+8838G>A
ENST00000441684.5:c.-274+3595G>A	ENSP00000412578.1:n.-274+3595G>A
ENST00000449576.6:c.139-15267G>A	ENSP00000397908.2:n.139-15267G>A
ENST00000495907.5:n.511+8115G>A
NM_001261427.1:c.9+8838G>A	NP_001248356.1:n.9+8838G>A
NM_001261428.1:c.139-15267G>A	NP_001248357.1:n.139-15267G>A
NM_001261429.1:c.9+8838G>A	NP_001248358.1:n.9+8838G>A
NM_145693.2:c.-10+3595G>A	NP_663731.1:n.-10+3595G>A
XM_006711869.1:c.139-15267G>A	XP_006711932.1:n.139-15267G>A
XM_006711870.2:c.9+8838G>A	XP_006711933.1:n.9+8838G>A
XM_006711871.1:c.-10+3595G>A	XP_006711934.1:n.-10+3595G>A
XM_006711872.1:c.-9-15267G>A	XP_006711935.1:n.-9-15267G>A
XM_011510333.1:c.139-15267G>A	XP_011508635.1:n.139-15267G>A
XM_011510334.1:c.9+8838G>A	XP_011508636.1:n.9+8838G>A
XM_011510335.1:c.-128+4065G>A	XP_011508637.1:n.-128+4065G>A
XM_011510336.1:c.-10+4065G>A	XP_011508638.1:n.-10+4065G>A
XM_011510337.1:c.139-15267G>A	XP_011508639.1:n.139-15267G>A
XM_011510338.1:c.139-15267G>A	XP_011508640.1:n.139-15267G>A
NM_001261427.2:c.9+8838G>A	NP_001248356.1:n.9+8838G>A
NM_001261428.2:c.139-15267G>A	NP_001248357.1:n.139-15267G>A
NM_001349199.1:c.-128+3595G>A	NP_001336128.1:n.-128+3595G>A
NM_001349200.1:c.-128+3595G>A	NP_001336129.1:n.-128+3595G>A
NM_001349201.1:c.-10+3595G>A	NP_001336130.1:n.-10+3595G>A
NM_001349202.1:c.-128+3595G>A	NP_001336131.1:n.-128+3595G>A
NM_001349203.1:c.-10+3595G>A	NP_001336132.1:n.-10+3595G>A
NM_001349204.1:c.-128+3595G>A	NP_001336133.1:n.-128+3595G>A
NM_001349205.1:c.-274+1526G>A	NP_001336134.1:n.-274+1526G>A
NM_001349206.1:c.-10+3595G>A	NP_001336135.1:n.-10+3595G>A
NM_001349207.1:c.82-15267G>A	NP_001336136.1:n.82-15267G>A
NM_001349208.1:c.139-15267G>A	NP_001336137.1:n.139-15267G>A
NM_145693.3:c.-10+3595G>A	NP_663731.1:n.-10+3595G>A
NR_146080.1:n.87+3595G>A
XM_006711870.4:c.9+8838G>A	XP_006711933.1:n.9+8838G>A
XM_006711872.3:c.-9-15267G>A	XP_006711935.1:n.-9-15267G>A
XM_011510333.2:c.139-15267G>A	XP_011508635.1:n.139-15267G>A
XM_011510334.3:c.9+8838G>A	XP_011508636.1:n.9+8838G>A
XM_011510335.3:c.-128+4065G>A	XP_011508637.1:n.-128+4065G>A
XM_011510336.3:c.-10+4065G>A	XP_011508638.1:n.-10+4065G>A
XM_017003623.2:c.61-15267G>A	XP_016859112.1:n.61-15267G>A
XM_017003624.2:c.-274+3595G>A	XP_016859113.1:n.-274+3595G>A
XM_017003627.2:c.-128+4065G>A	XP_016859116.1:n.-128+4065G>A
XM_017003628.2:c.-128+4065G>A	XP_016859117.1:n.-128+4065G>A
XM_017003629.1:c.-274+3595G>A	XP_016859118.1:n.-274+3595G>A
XM_024452762.1:c.-9-15267G>A	XP_024308530.1:n.-9-15267G>A
XM_024452763.1:c.9+8838G>A	XP_024308531.1:n.9+8838G>A
NM_001261428.3:c.139-15267G>A	NP_001248357.1:n.139-15267G>A
NM_001349199.2:c.-128+3595G>A	NP_001336128.1:n.-128+3595G>A
NM_001349200.2:c.-128+3595G>A	NP_001336129.1:n.-128+3595G>A
NM_001349201.2:c.-10+3595G>A	NP_001336130.1:n.-10+3595G>A
NM_001349202.2:c.-128+3595G>A	NP_001336131.1:n.-128+3595G>A
NM_001349203.2:c.-10+3595G>A	NP_001336132.1:n.-10+3595G>A
NM_001349204.2:c.-128+3595G>A	NP_001336133.1:n.-128+3595G>A
NM_001349206.2:c.-10+3595G>A MANE Select	NP_001336135.1:n.-10+3595G>A
NM_001349207.2:c.82-15267G>A	NP_001336136.1:n.82-15267G>A
NM_001349208.2:c.139-15267G>A	NP_001336137.1:n.139-15267G>A
NM_145693.4:c.-10+3595G>A	NP_663731.1:n.-10+3595G>A
NR_146080.2:n.40+3595G>A
NM_001261427.3:c.9+8838G>A	NP_001248356.1:n.9+8838G>A
NM_001349205.2:c.-274+1526G>A	NP_001336134.1:n.-274+1526G>A