Canonical Allele Identifier: CA2614950818

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72225137-CGTGGCGGGGGCCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225138_72225151del , CM000673.2:g.72225138_72225151del	GRCh38
NC_000011.9:g.71936182_71936195del , CM000673.1:g.71936182_71936195del	GRCh37
NC_000011.8:g.71613830_71613843del	NCBI36
NG_023253.1:g.5301_5314del
NG_023253.2:g.5301_5314del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.154_167del MANE Select	ENSP00000298229.2:p.Val52ArgfsTer18
ENST00000298229.6:c.154_167del	ENSP00000298229.2:p.Val52ArgfsTer18
ENST00000541544.1:n.70_83del
NM_001567.3:c.154_167del	NP_001558.3:p.Val52ArgfsTer18
XM_005273978.3:c.154_167del	XP_005274035.1:p.Val52ArgfsTer18
XM_005273979.3:c.154_167del	XP_005274036.1:p.Val52ArgfsTer18
XM_011544999.1:c.154_167del	XP_011543301.1:p.Val52ArgfsTer18
XM_011545000.1:c.154_167del	XP_011543302.1:p.Val52ArgfsTer18
XM_005273979.4:c.154_167del	XP_005274036.1:p.Val52ArgfsTer18
XM_011544999.2:c.154_167del	XP_011543301.1:p.Val52ArgfsTer18
XM_024448501.1:c.154_167del	XP_024304269.1:p.Val52ArgfsTer18
XM_024448502.1:c.154_167del	XP_024304270.1:p.Val52ArgfsTer18
XM_024448503.1:c.33_46del	XP_024304271.1:p.Trp12AlafsTer13
XM_024448504.1:c.154_167del	XP_024304272.1:p.Val52ArgfsTer18
XM_024448505.1:c.154_167del	XP_024304273.1:p.Val52ArgfsTer18
NM_001567.4:c.154_167del MANE Select	NP_001558.3:p.Val52ArgfsTer18