Canonical Allele Identifier: CA42574936
Gene: LPIN1 HGNC NCBI

Linked Data

dbSNP Id: rs144300109
gnomAD v2: 2-11890068-A-G
gnomAD v3: 2-11749942-A-G
gnomAD v4: 2-11749942-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11749942A>G , CM000664.2:g.11749942A>G GRCh38
NC_000002.11:g.11890068A>G , CM000664.1:g.11890068A>G GRCh37
NC_000002.10:g.11807519A>G NCBI36
NG_012843.2:g.77364A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000674199.1:c.-10+3271A>G MANE Select ENSP00000501331.1:n.-10+3271A>G
ENST00000256720.6:c.-10+3271A>G ENSP00000256720.2:n.-10+3271A>G
ENST00000396097.5:c.9+8514A>G ENSP00000379404.2:n.9+8514A>G
ENST00000396098.5:c.9+8514A>G ENSP00000379405.1:n.9+8514A>G
ENST00000396099.5:c.9+8514A>G ENSP00000379406.2:n.9+8514A>G
ENST00000423495.1:c.-360+3271A>G ENSP00000392424.1:n.-360+3271A>G
ENST00000425416.6:c.9+8514A>G ENSP00000401522.2:n.9+8514A>G
ENST00000441684.5:c.-274+3271A>G ENSP00000412578.1:n.-274+3271A>G
ENST00000449576.6:c.139-15591A>G ENSP00000397908.2:n.139-15591A>G
ENST00000495907.5:n.511+7791A>G
NM_001261427.1:c.9+8514A>G NP_001248356.1:n.9+8514A>G
NM_001261428.1:c.139-15591A>G NP_001248357.1:n.139-15591A>G
NM_001261429.1:c.9+8514A>G NP_001248358.1:n.9+8514A>G
NM_145693.2:c.-10+3271A>G NP_663731.1:n.-10+3271A>G
XM_006711869.1:c.139-15591A>G XP_006711932.1:n.139-15591A>G
XM_006711870.2:c.9+8514A>G XP_006711933.1:n.9+8514A>G
XM_006711871.1:c.-10+3271A>G XP_006711934.1:n.-10+3271A>G
XM_006711872.1:c.-9-15591A>G XP_006711935.1:n.-9-15591A>G
XM_011510333.1:c.139-15591A>G XP_011508635.1:n.139-15591A>G
XM_011510334.1:c.9+8514A>G XP_011508636.1:n.9+8514A>G
XM_011510335.1:c.-128+3741A>G XP_011508637.1:n.-128+3741A>G
XM_011510336.1:c.-10+3741A>G XP_011508638.1:n.-10+3741A>G
XM_011510337.1:c.139-15591A>G XP_011508639.1:n.139-15591A>G
XM_011510338.1:c.139-15591A>G XP_011508640.1:n.139-15591A>G
NM_001261427.2:c.9+8514A>G NP_001248356.1:n.9+8514A>G
NM_001261428.2:c.139-15591A>G NP_001248357.1:n.139-15591A>G
NM_001349199.1:c.-128+3271A>G NP_001336128.1:n.-128+3271A>G
NM_001349200.1:c.-128+3271A>G NP_001336129.1:n.-128+3271A>G
NM_001349201.1:c.-10+3271A>G NP_001336130.1:n.-10+3271A>G
NM_001349202.1:c.-128+3271A>G NP_001336131.1:n.-128+3271A>G
NM_001349203.1:c.-10+3271A>G NP_001336132.1:n.-10+3271A>G
NM_001349204.1:c.-128+3271A>G NP_001336133.1:n.-128+3271A>G
NM_001349205.1:c.-274+1202A>G NP_001336134.1:n.-274+1202A>G
NM_001349206.1:c.-10+3271A>G NP_001336135.1:n.-10+3271A>G
NM_001349207.1:c.82-15591A>G NP_001336136.1:n.82-15591A>G
NM_001349208.1:c.139-15591A>G NP_001336137.1:n.139-15591A>G
NM_145693.3:c.-10+3271A>G NP_663731.1:n.-10+3271A>G
NR_146080.1:n.87+3271A>G
XM_006711870.4:c.9+8514A>G XP_006711933.1:n.9+8514A>G
XM_006711872.3:c.-9-15591A>G XP_006711935.1:n.-9-15591A>G
XM_011510333.2:c.139-15591A>G XP_011508635.1:n.139-15591A>G
XM_011510334.3:c.9+8514A>G XP_011508636.1:n.9+8514A>G
XM_011510335.3:c.-128+3741A>G XP_011508637.1:n.-128+3741A>G
XM_011510336.3:c.-10+3741A>G XP_011508638.1:n.-10+3741A>G
XM_017003623.2:c.61-15591A>G XP_016859112.1:n.61-15591A>G
XM_017003624.2:c.-274+3271A>G XP_016859113.1:n.-274+3271A>G
XM_017003627.2:c.-128+3741A>G XP_016859116.1:n.-128+3741A>G
XM_017003628.2:c.-128+3741A>G XP_016859117.1:n.-128+3741A>G
XM_017003629.1:c.-274+3271A>G XP_016859118.1:n.-274+3271A>G
XM_024452762.1:c.-9-15591A>G XP_024308530.1:n.-9-15591A>G
XM_024452763.1:c.9+8514A>G XP_024308531.1:n.9+8514A>G
NM_001261428.3:c.139-15591A>G NP_001248357.1:n.139-15591A>G
NM_001349199.2:c.-128+3271A>G NP_001336128.1:n.-128+3271A>G
NM_001349200.2:c.-128+3271A>G NP_001336129.1:n.-128+3271A>G
NM_001349201.2:c.-10+3271A>G NP_001336130.1:n.-10+3271A>G
NM_001349202.2:c.-128+3271A>G NP_001336131.1:n.-128+3271A>G
NM_001349203.2:c.-10+3271A>G NP_001336132.1:n.-10+3271A>G
NM_001349204.2:c.-128+3271A>G NP_001336133.1:n.-128+3271A>G
NM_001349206.2:c.-10+3271A>G MANE Select NP_001336135.1:n.-10+3271A>G
NM_001349207.2:c.82-15591A>G NP_001336136.1:n.82-15591A>G
NM_001349208.2:c.139-15591A>G NP_001336137.1:n.139-15591A>G
NM_145693.4:c.-10+3271A>G NP_663731.1:n.-10+3271A>G
NR_146080.2:n.40+3271A>G
NM_001261427.3:c.9+8514A>G NP_001248356.1:n.9+8514A>G
NM_001349205.2:c.-274+1202A>G NP_001336134.1:n.-274+1202A>G