Canonical Allele Identifier: CA224379172

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72234763_72234764del , CM000673.2:g.72234763_72234764del	GRCh38
NC_000011.9:g.71945807_71945808del , CM000673.1:g.71945807_71945808del	GRCh37
NC_000011.8:g.71623455_71623456del	NCBI36
NG_023253.1:g.14926_14927del
NG_023253.2:g.14926_14927del

Transcript Alleles

HGVS	Amino-acid Change
NM_001567.4:c.2415+148_2415+149del MANE Select	NP_001558.3:n.2415+148_2415+149del
ENST00000298229.7:c.2415+148_2415+149del MANE Select	ENSP00000298229.2:n.2415+148_2415+149del
NM_001567.3:c.2415+148_2415+149del	NP_001558.3:n.2415+148_2415+149del
ENST00000298229.6:c.2415+148_2415+149del	ENSP00000298229.2:n.2415+148_2415+149del
ENST00000535985.1:c.268+148_268+149del
ENST00000538751.5:c.1689+148_1689+149del	ENSP00000444619.1:n.1689+148_1689+149del
ENST00000541303.5:n.1021+148_1021+149del
ENST00000541756.5:c.2217+148_2217+149del	ENSP00000446360.2:n.2217+148_2217+149del
ENST00000545355.5:n.700+148_700+149del
XM_005273978.3:c.2481+148_2481+149del	XP_005274035.1:n.2481+148_2481+149del
XM_005273979.3:c.2481+148_2481+149del	XP_005274036.1:n.2481+148_2481+149del
XM_005273979.4:c.2481+148_2481+149del	XP_005274036.1:n.2481+148_2481+149del
XM_011544999.1:c.2415+148_2415+149del	XP_011543301.1:n.2415+148_2415+149del
XM_011544999.2:c.2415+148_2415+149del	XP_011543301.1:n.2415+148_2415+149del
XM_011545000.1:c.2481+148_2481+149del	XP_011543302.1:n.2481+148_2481+149del
XM_024448501.1:c.2613+148_2613+149del	XP_024304269.1:n.2613+148_2613+149del
XM_024448502.1:c.2613+148_2613+149del	XP_024304270.1:n.2613+148_2613+149del
XM_024448503.1:c.2583+148_2583+149del	XP_024304271.1:n.2583+148_2583+149del
XM_024448504.1:c.2547+148_2547+149del	XP_024304272.1:n.2547+148_2547+149del
XM_024448505.1:c.2613+148_2613+149del	XP_024304273.1:n.2613+148_2613+149del