Canonical Allele Identifier: CA2489133762
Gene: LPIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11749981_11749983delinsAGT , CM000664.2:g.11749981_11749983delinsAGT GRCh38
NC_000002.11:g.11890107_11890109delinsAGT , CM000664.1:g.11890107_11890109delinsAGT GRCh37
NC_000002.10:g.11807558_11807560delinsAGT NCBI36
NG_012843.2:g.77403_77405delinsAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000674199.1:c.-10+3310_-10+3312delinsAGT MANE Select ENSP00000501331.1:n.-10+3310_-10+3312deli...
ENST00000256720.6:c.-10+3310_-10+3312delinsAGT ENSP00000256720.2:n.-10+3310_-10+3312deli...
ENST00000396097.5:c.9+8553_9+8555delinsAGT ENSP00000379404.2:n.9+8553_9+8555delinsAG...
ENST00000396098.5:c.9+8553_9+8555delinsAGT ENSP00000379405.1:n.9+8553_9+8555delinsAG...
ENST00000396099.5:c.9+8553_9+8555delinsAGT ENSP00000379406.2:n.9+8553_9+8555delinsAG...
ENST00000423495.1:c.-360+3310_-360+3312delinsAGT ENSP00000392424.1:n.-360+3310_-360+3312de...
ENST00000425416.6:c.9+8553_9+8555delinsAGT ENSP00000401522.2:n.9+8553_9+8555delinsAG...
ENST00000441684.5:c.-274+3310_-274+3312delinsAGT ENSP00000412578.1:n.-274+3310_-274+3312de...
ENST00000449576.6:c.139-15552_139-15550delinsAGT ENSP00000397908.2:n.139-15552_139-15550de...
ENST00000495907.5:n.511+7830_511+7832delinsAGT
NM_001261427.1:c.9+8553_9+8555delinsAGT NP_001248356.1:n.9+8553_9+8555delinsAGT
NM_001261428.1:c.139-15552_139-15550delinsAGT NP_001248357.1:n.139-15552_139-15550delin...
NM_001261429.1:c.9+8553_9+8555delinsAGT NP_001248358.1:n.9+8553_9+8555delinsAGT
NM_145693.2:c.-10+3310_-10+3312delinsAGT NP_663731.1:n.-10+3310_-10+3312delinsAGT
XM_006711869.1:c.139-15552_139-15550delinsAGT XP_006711932.1:n.139-15552_139-15550delin...
XM_006711870.2:c.9+8553_9+8555delinsAGT XP_006711933.1:n.9+8553_9+8555delinsAGT
XM_006711871.1:c.-10+3310_-10+3312delinsAGT XP_006711934.1:n.-10+3310_-10+3312delinsA...
XM_006711872.1:c.-9-15552_-9-15550delinsAGT XP_006711935.1:n.-9-15552_-9-15550delinsA...
XM_011510333.1:c.139-15552_139-15550delinsAGT XP_011508635.1:n.139-15552_139-15550delin...
XM_011510334.1:c.9+8553_9+8555delinsAGT XP_011508636.1:n.9+8553_9+8555delinsAGT
XM_011510335.1:c.-128+3780_-128+3782delinsAGT XP_011508637.1:n.-128+3780_-128+3782delin...
XM_011510336.1:c.-10+3780_-10+3782delinsAGT XP_011508638.1:n.-10+3780_-10+3782delinsA...
XM_011510337.1:c.139-15552_139-15550delinsAGT XP_011508639.1:n.139-15552_139-15550delin...
XM_011510338.1:c.139-15552_139-15550delinsAGT XP_011508640.1:n.139-15552_139-15550delin...
NM_001261427.2:c.9+8553_9+8555delinsAGT NP_001248356.1:n.9+8553_9+8555delinsAGT
NM_001261428.2:c.139-15552_139-15550delinsAGT NP_001248357.1:n.139-15552_139-15550delin...
NM_001349199.1:c.-128+3310_-128+3312delinsAGT NP_001336128.1:n.-128+3310_-128+3312delin...
NM_001349200.1:c.-128+3310_-128+3312delinsAGT NP_001336129.1:n.-128+3310_-128+3312delin...
NM_001349201.1:c.-10+3310_-10+3312delinsAGT NP_001336130.1:n.-10+3310_-10+3312delinsA...
NM_001349202.1:c.-128+3310_-128+3312delinsAGT NP_001336131.1:n.-128+3310_-128+3312delin...
NM_001349203.1:c.-10+3310_-10+3312delinsAGT NP_001336132.1:n.-10+3310_-10+3312delinsA...
NM_001349204.1:c.-128+3310_-128+3312delinsAGT NP_001336133.1:n.-128+3310_-128+3312delin...
NM_001349205.1:c.-274+1241_-274+1243delinsAGT NP_001336134.1:n.-274+1241_-274+1243delin...
NM_001349206.1:c.-10+3310_-10+3312delinsAGT NP_001336135.1:n.-10+3310_-10+3312delinsA...
NM_001349207.1:c.82-15552_82-15550delinsAGT NP_001336136.1:n.82-15552_82-15550delinsA...
NM_001349208.1:c.139-15552_139-15550delinsAGT NP_001336137.1:n.139-15552_139-15550delin...
NM_145693.3:c.-10+3310_-10+3312delinsAGT NP_663731.1:n.-10+3310_-10+3312delinsAGT
NR_146080.1:n.87+3310_87+3312delinsAGT
XM_006711870.4:c.9+8553_9+8555delinsAGT XP_006711933.1:n.9+8553_9+8555delinsAGT
XM_006711872.3:c.-9-15552_-9-15550delinsAGT XP_006711935.1:n.-9-15552_-9-15550delinsA...
XM_011510333.2:c.139-15552_139-15550delinsAGT XP_011508635.1:n.139-15552_139-15550delin...
XM_011510334.3:c.9+8553_9+8555delinsAGT XP_011508636.1:n.9+8553_9+8555delinsAGT
XM_011510335.3:c.-128+3780_-128+3782delinsAGT XP_011508637.1:n.-128+3780_-128+3782delin...
XM_011510336.3:c.-10+3780_-10+3782delinsAGT XP_011508638.1:n.-10+3780_-10+3782delinsA...
XM_017003623.2:c.61-15552_61-15550delinsAGT XP_016859112.1:n.61-15552_61-15550delinsA...
XM_017003624.2:c.-274+3310_-274+3312delinsAGT XP_016859113.1:n.-274+3310_-274+3312delin...
XM_017003627.2:c.-128+3780_-128+3782delinsAGT XP_016859116.1:n.-128+3780_-128+3782delin...
XM_017003628.2:c.-128+3780_-128+3782delinsAGT XP_016859117.1:n.-128+3780_-128+3782delin...
XM_017003629.1:c.-274+3310_-274+3312delinsAGT XP_016859118.1:n.-274+3310_-274+3312delin...
XM_024452762.1:c.-9-15552_-9-15550delinsAGT XP_024308530.1:n.-9-15552_-9-15550delinsA...
XM_024452763.1:c.9+8553_9+8555delinsAGT XP_024308531.1:n.9+8553_9+8555delinsAGT
NM_001261428.3:c.139-15552_139-15550delinsAGT NP_001248357.1:n.139-15552_139-15550delin...
NM_001349199.2:c.-128+3310_-128+3312delinsAGT NP_001336128.1:n.-128+3310_-128+3312delin...
NM_001349200.2:c.-128+3310_-128+3312delinsAGT NP_001336129.1:n.-128+3310_-128+3312delin...
NM_001349201.2:c.-10+3310_-10+3312delinsAGT NP_001336130.1:n.-10+3310_-10+3312delinsA...
NM_001349202.2:c.-128+3310_-128+3312delinsAGT NP_001336131.1:n.-128+3310_-128+3312delin...
NM_001349203.2:c.-10+3310_-10+3312delinsAGT NP_001336132.1:n.-10+3310_-10+3312delinsA...
NM_001349204.2:c.-128+3310_-128+3312delinsAGT NP_001336133.1:n.-128+3310_-128+3312delin...
NM_001349206.2:c.-10+3310_-10+3312delinsAGT MANE Select NP_001336135.1:n.-10+3310_-10+3312delinsA...
NM_001349207.2:c.82-15552_82-15550delinsAGT NP_001336136.1:n.82-15552_82-15550delinsA...
NM_001349208.2:c.139-15552_139-15550delinsAGT NP_001336137.1:n.139-15552_139-15550delin...
NM_145693.4:c.-10+3310_-10+3312delinsAGT NP_663731.1:n.-10+3310_-10+3312delinsAGT
NR_146080.2:n.40+3310_40+3312delinsAGT
NM_001261427.3:c.9+8553_9+8555delinsAGT NP_001248356.1:n.9+8553_9+8555delinsAGT
NM_001349205.2:c.-274+1241_-274+1243delinsAGT NP_001336134.1:n.-274+1241_-274+1243delin...