Canonical Allele Identifier: CA1981897852

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229967_72229968delinsCT , CM000673.2:g.72229967_72229968delinsCT	GRCh38
NC_000011.9:g.71941011_71941012delinsCT , CM000673.1:g.71941011_71941012delinsCT	GRCh37
NC_000011.8:g.71618659_71618660delinsCT	NCBI36
NG_023253.1:g.10130_10131delinsCT
NG_023253.2:g.10130_10131delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.887_888delinsCT MANE Select	ENSP00000298229.2:p.Ala296=
ENST00000298229.6:c.887_888delinsCT	ENSP00000298229.2:p.Ala296=
ENST00000538751.5:c.161_162delinsCT	ENSP00000444619.1:p.Ala54=
ENST00000540329.5:c.71_72delinsCT	ENSP00000440018.1:p.Ala24=
ENST00000541756.5:c.689_690delinsCT	ENSP00000446360.2:p.Ala230=
NM_001567.3:c.887_888delinsCT	NP_001558.3:p.Ala296=
XM_005273978.3:c.953_954delinsCT	XP_005274035.1:p.Ala318=
XM_005273979.3:c.953_954delinsCT	XP_005274036.1:p.Ala318=
XM_011544999.1:c.887_888delinsCT	XP_011543301.1:p.Ala296=
XM_011545000.1:c.953_954delinsCT	XP_011543302.1:p.Ala318=
XM_005273979.4:c.953_954delinsCT	XP_005274036.1:p.Ala318=
XM_011544999.2:c.887_888delinsCT	XP_011543301.1:p.Ala296=
XM_024448501.1:c.953_954delinsCT	XP_024304269.1:p.Ala318=
XM_024448502.1:c.953_954delinsCT	XP_024304270.1:p.Ala318=
XM_024448503.1:c.923_924delinsCT	XP_024304271.1:p.Ala308=
XM_024448504.1:c.887_888delinsCT	XP_024304272.1:p.Ala296=
XM_024448505.1:c.953_954delinsCT	XP_024304273.1:p.Ala318=
NM_001567.4:c.887_888delinsCT MANE Select	NP_001558.3:p.Ala296=