Canonical Allele Identifier: CA2657935575

Gene: LPIN1

Linked Data

• gnomAD v4: 2-11771681-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11771683del , CM000664.2:g.11771683del	GRCh38
NC_000002.11:g.11911809del , CM000664.1:g.11911809del	GRCh37
NC_000002.10:g.11829260del	NCBI36
NG_012843.2:g.99105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674199.1:c.596+4del MANE Select	ENSP00000501331.1:n.596+4del
ENST00000256720.6:c.596+4del	ENSP00000256720.2:n.596+4del
ENST00000396097.5:c.614+4del	ENSP00000379404.2:n.614+4del
ENST00000396098.5:c.614+4del	ENSP00000379405.1:n.614+4del
ENST00000396099.5:c.614+4del	ENSP00000379406.2:n.614+4del
ENST00000425416.6:c.614+4del	ENSP00000401522.2:n.614+4del
ENST00000449576.6:c.743+4del	ENSP00000397908.2:n.743+4del
NM_001261427.1:c.614+4del	NP_001248356.1:n.614+4del
NM_001261428.1:c.743+4del	NP_001248357.1:n.743+4del
NM_001261429.1:c.614+4del	NP_001248358.1:n.614+4del
NM_145693.2:c.596+4del	NP_663731.1:n.596+4del
XM_006711869.1:c.743+4del	XP_006711932.1:n.743+4del
XM_006711870.2:c.614+4del	XP_006711933.1:n.614+4del
XM_006711871.1:c.596+4del	XP_006711934.1:n.596+4del
XM_006711872.1:c.596+4del	XP_006711935.1:n.596+4del
XM_006711874.1:c.596+4del	XP_006711937.1:n.596+4del
XM_011510333.1:c.743+4del	XP_011508635.1:n.743+4del
XM_011510334.1:c.614+4del	XP_011508636.1:n.614+4del
XM_011510335.1:c.596+4del	XP_011508637.1:n.596+4del
XM_011510336.1:c.596+4del	XP_011508638.1:n.596+4del
XM_011510337.1:c.743+4del	XP_011508639.1:n.743+4del
XM_011510338.1:c.743+4del	XP_011508640.1:n.743+4del
NM_001261427.2:c.614+4del	NP_001248356.1:n.614+4del
NM_001261428.2:c.743+4del	NP_001248357.1:n.743+4del
NM_001349199.1:c.596+4del	NP_001336128.1:n.596+4del
NM_001349200.1:c.596+4del	NP_001336129.1:n.596+4del
NM_001349201.1:c.596+4del	NP_001336130.1:n.596+4del
NM_001349202.1:c.596+4del	NP_001336131.1:n.596+4del
NM_001349203.1:c.596+4del	NP_001336132.1:n.596+4del
NM_001349204.1:c.596+4del	NP_001336133.1:n.596+4del
NM_001349205.1:c.596+4del	NP_001336134.1:n.596+4del
NM_001349206.1:c.596+4del	NP_001336135.1:n.596+4del
NM_001349207.1:c.686+4del	NP_001336136.1:n.686+4del
NM_001349208.1:c.743+4del	NP_001336137.1:n.743+4del
NM_145693.3:c.596+4del	NP_663731.1:n.596+4del
NR_146080.1:n.692+4del
XM_006711870.4:c.614+4del	XP_006711933.1:n.614+4del
XM_006711872.3:c.596+4del	XP_006711935.1:n.596+4del
XM_011510333.2:c.743+4del	XP_011508635.1:n.743+4del
XM_011510334.3:c.614+4del	XP_011508636.1:n.614+4del
XM_011510335.3:c.596+4del	XP_011508637.1:n.596+4del
XM_011510336.3:c.596+4del	XP_011508638.1:n.596+4del
XM_017003623.2:c.665+4del	XP_016859112.1:n.665+4del
XM_017003624.2:c.596+4del	XP_016859113.1:n.596+4del
XM_017003625.2:c.596+4del	XP_016859114.1:n.596+4del
XM_017003627.2:c.596+4del	XP_016859116.1:n.596+4del
XM_017003628.2:c.596+4del	XP_016859117.1:n.596+4del
XM_017003629.1:c.596+4del	XP_016859118.1:n.596+4del
XM_017003630.2:c.596+4del	XP_016859119.1:n.596+4del
XM_017003631.1:c.596+4del	XP_016859120.1:n.596+4del
XM_024452762.1:c.596+4del	XP_024308530.1:n.596+4del
XM_024452763.1:c.614+4del	XP_024308531.1:n.614+4del
NM_001261428.3:c.743+4del	NP_001248357.1:n.743+4del
NM_001349199.2:c.596+4del	NP_001336128.1:n.596+4del
NM_001349200.2:c.596+4del	NP_001336129.1:n.596+4del
NM_001349201.2:c.596+4del	NP_001336130.1:n.596+4del
NM_001349202.2:c.596+4del	NP_001336131.1:n.596+4del
NM_001349203.2:c.596+4del	NP_001336132.1:n.596+4del
NM_001349204.2:c.596+4del	NP_001336133.1:n.596+4del
NM_001349206.2:c.596+4del MANE Select	NP_001336135.1:n.596+4del
NM_001349207.2:c.686+4del	NP_001336136.1:n.686+4del
NM_001349208.2:c.743+4del	NP_001336137.1:n.743+4del
NM_145693.4:c.596+4del	NP_663731.1:n.596+4del
NR_146080.2:n.645+4del
NM_001261427.3:c.614+4del	NP_001248356.1:n.614+4del
NM_001349205.2:c.596+4del	NP_001336134.1:n.596+4del