Canonical Allele Identifier: CA600085273

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72234759_72234764dup , CM000673.2:g.72234759_72234764dup	GRCh38
NC_000011.9:g.71945803_71945808dup , CM000673.1:g.71945803_71945808dup	GRCh37
NC_000011.8:g.71623451_71623456dup	NCBI36
NG_023253.1:g.14922_14927dup
NG_023253.2:g.14922_14927dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.2415+144_2415+149dup MANE Select	ENSP00000298229.2:n.2415+144_2415+149dup
ENST00000298229.6:c.2415+144_2415+149dup	ENSP00000298229.2:n.2415+144_2415+149dup
ENST00000535985.1:c.268+144_268+149dup
ENST00000538751.5:c.1689+144_1689+149dup	ENSP00000444619.1:n.1689+144_1689+149dup
ENST00000541303.5:n.1021+144_1021+149dup
ENST00000541756.5:c.2217+144_2217+149dup	ENSP00000446360.2:n.2217+144_2217+149dup
ENST00000545355.5:n.700+144_700+149dup
NM_001567.3:c.2415+144_2415+149dup	NP_001558.3:n.2415+144_2415+149dup
XM_005273978.3:c.2481+144_2481+149dup	XP_005274035.1:n.2481+144_2481+149dup
XM_005273979.3:c.2481+144_2481+149dup	XP_005274036.1:n.2481+144_2481+149dup
XM_011544999.1:c.2415+144_2415+149dup	XP_011543301.1:n.2415+144_2415+149dup
XM_011545000.1:c.2481+144_2481+149dup	XP_011543302.1:n.2481+144_2481+149dup
XM_005273979.4:c.2481+144_2481+149dup	XP_005274036.1:n.2481+144_2481+149dup
XM_011544999.2:c.2415+144_2415+149dup	XP_011543301.1:n.2415+144_2415+149dup
XM_024448501.1:c.2613+144_2613+149dup	XP_024304269.1:n.2613+144_2613+149dup
XM_024448502.1:c.2613+144_2613+149dup	XP_024304270.1:n.2613+144_2613+149dup
XM_024448503.1:c.2583+144_2583+149dup	XP_024304271.1:n.2583+144_2583+149dup
XM_024448504.1:c.2547+144_2547+149dup	XP_024304272.1:n.2547+144_2547+149dup
XM_024448505.1:c.2613+144_2613+149dup	XP_024304273.1:n.2613+144_2613+149dup
NM_001567.4:c.2415+144_2415+149dup MANE Select	NP_001558.3:n.2415+144_2415+149dup