Canonical Allele Identifier: CA212823

Gene: LPIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11785078T>C , CM000664.2:g.11785078T>C	GRCh38
NC_000002.11:g.11925204T>C , CM000664.1:g.11925204T>C	GRCh37
NC_000002.10:g.11842655T>C	NCBI36
NG_012843.2:g.112500T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674199.1:c.1549+2T>C MANE Select	ENSP00000501331.1:n.1549+2T>C
ENST00000256720.6:c.1441+2T>C	ENSP00000256720.2:n.1441+2T>C
ENST00000396097.5:c.1567+2T>C	ENSP00000379404.2:n.1567+2T>C
ENST00000396099.5:c.1567+2T>C	ENSP00000379406.2:n.1567+2T>C
ENST00000404113.6:n.1034+2T>C
ENST00000425416.6:c.1459+2T>C	ENSP00000401522.2:n.1459+2T>C
ENST00000449576.6:c.1696+2T>C	ENSP00000397908.2:n.1696+2T>C
NM_001261427.1:c.1459+2T>C	NP_001248356.1:n.1459+2T>C
NM_001261428.1:c.1696+2T>C	NP_001248357.1:n.1696+2T>C
NM_145693.2:c.1441+2T>C	NP_663731.1:n.1441+2T>C
XM_006711869.1:c.1588+2T>C	XP_006711932.1:n.1588+2T>C
XM_006711870.2:c.1567+2T>C	XP_006711933.1:n.1567+2T>C
XM_006711871.1:c.1549+2T>C	XP_006711934.1:n.1549+2T>C
XM_006711872.1:c.1549+2T>C	XP_006711935.1:n.1549+2T>C
XM_006711874.1:c.1549+2T>C	XP_006711937.1:n.1549+2T>C
XM_011510333.1:c.1693+2T>C	XP_011508635.1:n.1693+2T>C
XM_011510334.1:c.1567+2T>C	XP_011508636.1:n.1567+2T>C
XM_011510335.1:c.1549+2T>C	XP_011508637.1:n.1549+2T>C
XM_011510336.1:c.1549+2T>C	XP_011508638.1:n.1549+2T>C
XM_011510337.1:c.1696+2T>C	XP_011508639.1:n.1696+2T>C
NM_001261427.2:c.1459+2T>C	NP_001248356.1:n.1459+2T>C
NM_001261428.2:c.1696+2T>C	NP_001248357.1:n.1696+2T>C
NM_001349199.1:c.1441+2T>C	NP_001336128.1:n.1441+2T>C
NM_001349200.1:c.1441+2T>C	NP_001336129.1:n.1441+2T>C
NM_001349201.1:c.1441+2T>C	NP_001336130.1:n.1441+2T>C
NM_001349202.1:c.1546+2T>C	NP_001336131.1:n.1546+2T>C
NM_001349203.1:c.1546+2T>C	NP_001336132.1:n.1546+2T>C
NM_001349204.1:c.1549+2T>C	NP_001336133.1:n.1549+2T>C
NM_001349205.1:c.1549+2T>C	NP_001336134.1:n.1549+2T>C
NM_001349206.1:c.1549+2T>C	NP_001336135.1:n.1549+2T>C
NM_001349207.1:c.1639+2T>C	NP_001336136.1:n.1639+2T>C
NM_001349208.1:c.1588+2T>C	NP_001336137.1:n.1588+2T>C
NM_145693.3:c.1441+2T>C	NP_663731.1:n.1441+2T>C
NR_146080.1:n.1537+2T>C
XM_006711870.4:c.1567+2T>C	XP_006711933.1:n.1567+2T>C
XM_006711872.3:c.1549+2T>C	XP_006711935.1:n.1549+2T>C
XM_011510333.2:c.1693+2T>C	XP_011508635.1:n.1693+2T>C
XM_011510334.3:c.1567+2T>C	XP_011508636.1:n.1567+2T>C
XM_011510335.3:c.1549+2T>C	XP_011508637.1:n.1549+2T>C
XM_011510336.3:c.1549+2T>C	XP_011508638.1:n.1549+2T>C
XM_017003623.2:c.1618+2T>C	XP_016859112.1:n.1618+2T>C
XM_017003624.2:c.1549+2T>C	XP_016859113.1:n.1549+2T>C
XM_017003625.2:c.1549+2T>C	XP_016859114.1:n.1549+2T>C
XM_017003627.2:c.1546+2T>C	XP_016859116.1:n.1546+2T>C
XM_017003628.2:c.1441+2T>C	XP_016859117.1:n.1441+2T>C
XM_017003629.1:c.1441+2T>C	XP_016859118.1:n.1441+2T>C
XM_017003630.2:c.1441+2T>C	XP_016859119.1:n.1441+2T>C
XM_024452762.1:c.1549+2T>C	XP_024308530.1:n.1549+2T>C
XM_024452763.1:c.1459+2T>C	XP_024308531.1:n.1459+2T>C
NM_001261428.3:c.1696+2T>C	NP_001248357.1:n.1696+2T>C
NM_001349199.2:c.1441+2T>C	NP_001336128.1:n.1441+2T>C
NM_001349200.2:c.1441+2T>C	NP_001336129.1:n.1441+2T>C
NM_001349201.2:c.1441+2T>C	NP_001336130.1:n.1441+2T>C
NM_001349202.2:c.1546+2T>C	NP_001336131.1:n.1546+2T>C
NM_001349203.2:c.1546+2T>C	NP_001336132.1:n.1546+2T>C
NM_001349204.2:c.1549+2T>C	NP_001336133.1:n.1549+2T>C
NM_001349206.2:c.1549+2T>C MANE Select	NP_001336135.1:n.1549+2T>C
NM_001349207.2:c.1639+2T>C	NP_001336136.1:n.1639+2T>C
NM_001349208.2:c.1588+2T>C	NP_001336137.1:n.1588+2T>C
NM_145693.4:c.1441+2T>C	NP_663731.1:n.1441+2T>C
NR_146080.2:n.1490+2T>C
NM_001261427.3:c.1459+2T>C	NP_001248356.1:n.1459+2T>C
NM_001349205.2:c.1549+2T>C	NP_001336134.1:n.1549+2T>C