Canonical Allele Identifier: CA11333066
Gene: LPIN1 HGNC NCBI

Linked Data

dbSNP Id: rs11693809

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11750012T>C , CM000664.2:g.11750012T>C GRCh38
NC_000002.11:g.11890138T>C , CM000664.1:g.11890138T>C GRCh37
NC_000002.10:g.11807589T>C NCBI36
NG_012843.2:g.77434T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000674199.1:c.-10+3341T>C MANE Select ENSP00000501331.1:p.=
ENST00000256720.6:c.-10+3341T>C ENSP00000256720.2:p.=
ENST00000396097.5:c.9+8584T>C ENSP00000379404.2:p.=
ENST00000396098.5:c.9+8584T>C ENSP00000379405.1:p.=
ENST00000396099.5:c.9+8584T>C ENSP00000379406.2:p.=
ENST00000423495.1:c.-360+3341T>C ENSP00000392424.1:p.=
ENST00000425416.6:c.9+8584T>C ENSP00000401522.2:p.=
ENST00000441684.5:c.-274+3341T>C ENSP00000412578.1:p.=
ENST00000449576.6:c.139-15521T>C ENSP00000397908.2:p.=
ENST00000495907.5:n.511+7861T>C
NM_001261427.1:c.9+8584T>C NP_001248356.1:p.=
NM_001261428.1:c.139-15521T>C NP_001248357.1:p.=
NM_001261429.1:c.9+8584T>C NP_001248358.1:p.=
NM_145693.2:c.-10+3341T>C NP_663731.1:p.=
XM_006711869.1:c.139-15521T>C XP_006711932.1:p.=
XM_006711870.2:c.9+8584T>C XP_006711933.1:p.=
XM_006711871.1:c.-10+3341T>C XP_006711934.1:p.=
XM_006711872.1:c.-9-15521T>C XP_006711935.1:p.=
XM_011510333.1:c.139-15521T>C XP_011508635.1:p.=
XM_011510334.1:c.9+8584T>C XP_011508636.1:p.=
XM_011510335.1:c.-128+3811T>C XP_011508637.1:p.=
XM_011510336.1:c.-10+3811T>C XP_011508638.1:p.=
XM_011510337.1:c.139-15521T>C XP_011508639.1:p.=
XM_011510338.1:c.139-15521T>C XP_011508640.1:p.=
NM_001261427.2:c.9+8584T>C NP_001248356.1:p.=
NM_001261428.2:c.139-15521T>C NP_001248357.1:p.=
NM_001349199.1:c.-128+3341T>C NP_001336128.1:p.=
NM_001349200.1:c.-128+3341T>C NP_001336129.1:p.=
NM_001349201.1:c.-10+3341T>C NP_001336130.1:p.=
NM_001349202.1:c.-128+3341T>C NP_001336131.1:p.=
NM_001349203.1:c.-10+3341T>C NP_001336132.1:p.=
NM_001349204.1:c.-128+3341T>C NP_001336133.1:p.=
NM_001349205.1:c.-274+1272T>C NP_001336134.1:p.=
NM_001349206.1:c.-10+3341T>C NP_001336135.1:p.=
NM_001349207.1:c.82-15521T>C NP_001336136.1:p.=
NM_001349208.1:c.139-15521T>C NP_001336137.1:p.=
NM_145693.3:c.-10+3341T>C NP_663731.1:p.=
NR_146080.1:n.87+3341T>C
XM_006711870.4:c.9+8584T>C XP_006711933.1:p.=
XM_006711872.3:c.-9-15521T>C XP_006711935.1:p.=
XM_011510333.2:c.139-15521T>C XP_011508635.1:p.=
XM_011510334.3:c.9+8584T>C XP_011508636.1:p.=
XM_011510335.3:c.-128+3811T>C XP_011508637.1:p.=
XM_011510336.3:c.-10+3811T>C XP_011508638.1:p.=
XM_017003623.2:c.61-15521T>C XP_016859112.1:p.=
XM_017003624.2:c.-274+3341T>C XP_016859113.1:p.=
XM_017003627.2:c.-128+3811T>C XP_016859116.1:p.=
XM_017003628.2:c.-128+3811T>C XP_016859117.1:p.=
XM_017003629.1:c.-274+3341T>C XP_016859118.1:p.=
XM_024452762.1:c.-9-15521T>C XP_024308530.1:p.=
XM_024452763.1:c.9+8584T>C XP_024308531.1:p.=
NM_001261428.3:c.139-15521T>C NP_001248357.1:p.=
NM_001349199.2:c.-128+3341T>C NP_001336128.1:p.=
NM_001349200.2:c.-128+3341T>C NP_001336129.1:p.=
NM_001349201.2:c.-10+3341T>C NP_001336130.1:p.=
NM_001349202.2:c.-128+3341T>C NP_001336131.1:p.=
NM_001349203.2:c.-10+3341T>C NP_001336132.1:p.=
NM_001349204.2:c.-128+3341T>C NP_001336133.1:p.=
NM_001349206.2:c.-10+3341T>C MANE Select NP_001336135.1:p.=
NM_001349207.2:c.82-15521T>C NP_001336136.1:p.=
NM_001349208.2:c.139-15521T>C NP_001336137.1:p.=
NM_145693.4:c.-10+3341T>C NP_663731.1:p.=
NR_146080.2:n.40+3341T>C
NM_001261427.3:c.9+8584T>C NP_001248356.1:p.=
NM_001349205.2:c.-274+1272T>C NP_001336134.1:p.=