Canonical Allele Identifier: CA42604558

Gene: LPIN1

Linked Data

• dbSNP Id: rs901370069
• MyVariant Identifiers: chr2:g.11923976G>A (hg19) ; chr2:g.11783850G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11783850G>A , CM000664.2:g.11783850G>A	GRCh38
NC_000002.11:g.11923976G>A , CM000664.1:g.11923976G>A	GRCh37
NC_000002.10:g.11841427G>A	NCBI36
NG_012843.2:g.111272G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674199.1:c.1286G>A MANE Select	ENSP00000501331.1:p.Gly429Asp
ENST00000256720.6:c.1178G>A	ENSP00000256720.2:p.Gly393Asp
ENST00000396097.5:c.1304G>A	ENSP00000379404.2:p.Gly435Asp
ENST00000396098.5:c.1304G>A	ENSP00000379405.1:p.Gly435Asp
ENST00000396099.5:c.1304G>A	ENSP00000379406.2:p.Gly435Asp
ENST00000404113.6:n.771G>A
ENST00000425416.6:c.1196G>A	ENSP00000401522.2:p.Gly399Asp
ENST00000449576.6:c.1433G>A	ENSP00000397908.2:p.Gly478Asp
ENST00000460096.1:n.166G>A
NM_001261427.1:c.1196G>A	NP_001248356.1:p.Gly399Asp
NM_001261428.1:c.1433G>A	NP_001248357.1:p.Gly478Asp
NM_001261429.1:c.1304G>A	NP_001248358.1:p.Gly435Asp
NM_145693.2:c.1178G>A	NP_663731.1:p.Gly393Asp
XM_006711869.1:c.1325G>A	XP_006711932.1:p.Gly442Asp
XM_006711870.2:c.1304G>A	XP_006711933.1:p.Gly435Asp
XM_006711871.1:c.1286G>A	XP_006711934.1:p.Gly429Asp
XM_006711872.1:c.1286G>A	XP_006711935.1:p.Gly429Asp
XM_006711874.1:c.1286G>A	XP_006711937.1:p.Gly429Asp
XM_011510333.1:c.1430G>A	XP_011508635.1:p.Gly477Asp
XM_011510334.1:c.1304G>A	XP_011508636.1:p.Gly435Asp
XM_011510335.1:c.1286G>A	XP_011508637.1:p.Gly429Asp
XM_011510336.1:c.1286G>A	XP_011508638.1:p.Gly429Asp
XM_011510337.1:c.1433G>A	XP_011508639.1:p.Gly478Asp
XM_011510338.1:c.1433G>A	XP_011508640.1:p.Gly478Asp
NM_001261427.2:c.1196G>A	NP_001248356.1:p.Gly399Asp
NM_001261428.2:c.1433G>A	NP_001248357.1:p.Gly478Asp
NM_001349199.1:c.1178G>A	NP_001336128.1:p.Gly393Asp
NM_001349200.1:c.1178G>A	NP_001336129.1:p.Gly393Asp
NM_001349201.1:c.1178G>A	NP_001336130.1:p.Gly393Asp
NM_001349202.1:c.1283G>A	NP_001336131.1:p.Gly428Asp
NM_001349203.1:c.1283G>A	NP_001336132.1:p.Gly428Asp
NM_001349204.1:c.1286G>A	NP_001336133.1:p.Gly429Asp
NM_001349205.1:c.1286G>A	NP_001336134.1:p.Gly429Asp
NM_001349206.1:c.1286G>A	NP_001336135.1:p.Gly429Asp
NM_001349207.1:c.1376G>A	NP_001336136.1:p.Gly459Asp
NM_001349208.1:c.1325G>A	NP_001336137.1:p.Gly442Asp
NM_145693.3:c.1178G>A	NP_663731.1:p.Gly393Asp
NR_146080.1:n.1274G>A
XM_006711870.4:c.1304G>A	XP_006711933.1:p.Gly435Asp
XM_006711872.3:c.1286G>A	XP_006711935.1:p.Gly429Asp
XM_011510333.2:c.1430G>A	XP_011508635.1:p.Gly477Asp
XM_011510334.3:c.1304G>A	XP_011508636.1:p.Gly435Asp
XM_011510335.3:c.1286G>A	XP_011508637.1:p.Gly429Asp
XM_011510336.3:c.1286G>A	XP_011508638.1:p.Gly429Asp
XM_017003623.2:c.1355G>A	XP_016859112.1:p.Gly452Asp
XM_017003624.2:c.1286G>A	XP_016859113.1:p.Gly429Asp
XM_017003625.2:c.1286G>A	XP_016859114.1:p.Gly429Asp
XM_017003627.2:c.1283G>A	XP_016859116.1:p.Gly428Asp
XM_017003628.2:c.1178G>A	XP_016859117.1:p.Gly393Asp
XM_017003629.1:c.1178G>A	XP_016859118.1:p.Gly393Asp
XM_017003630.2:c.1178G>A	XP_016859119.1:p.Gly393Asp
XM_017003631.1:c.1286G>A	XP_016859120.1:p.Gly429Asp
XM_024452762.1:c.1286G>A	XP_024308530.1:p.Gly429Asp
XM_024452763.1:c.1196G>A	XP_024308531.1:p.Gly399Asp
NM_001261428.3:c.1433G>A	NP_001248357.1:p.Gly478Asp
NM_001349199.2:c.1178G>A	NP_001336128.1:p.Gly393Asp
NM_001349200.2:c.1178G>A	NP_001336129.1:p.Gly393Asp
NM_001349201.2:c.1178G>A	NP_001336130.1:p.Gly393Asp
NM_001349202.2:c.1283G>A	NP_001336131.1:p.Gly428Asp
NM_001349203.2:c.1283G>A	NP_001336132.1:p.Gly428Asp
NM_001349204.2:c.1286G>A	NP_001336133.1:p.Gly429Asp
NM_001349206.2:c.1286G>A MANE Select	NP_001336135.1:p.Gly429Asp
NM_001349207.2:c.1376G>A	NP_001336136.1:p.Gly459Asp
NM_001349208.2:c.1325G>A	NP_001336137.1:p.Gly442Asp
NM_145693.4:c.1178G>A	NP_663731.1:p.Gly393Asp
NR_146080.2:n.1227G>A
NM_001261427.3:c.1196G>A	NP_001248356.1:p.Gly399Asp
NM_001349205.2:c.1286G>A	NP_001336134.1:p.Gly429Asp