Canonical Allele Identifier: CA1981897988

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230258C= , CM000673.2:g.72230258C=	GRCh38
NC_000011.9:g.71941302C= , CM000673.1:g.71941302C=	GRCh37
NC_000011.8:g.71618950C=	NCBI36
NG_023253.1:g.10421C=
NG_023253.2:g.10421C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1077C= MANE Select	ENSP00000298229.2:p.Phe359=
ENST00000298229.6:c.1077C=	ENSP00000298229.2:p.Phe359=
ENST00000538751.5:c.351C=	ENSP00000444619.1:p.Phe117=
ENST00000540329.5:c.261C=	ENSP00000440018.1:p.Phe87=
ENST00000541756.5:c.879C=	ENSP00000446360.2:p.Phe293=
NM_001567.3:c.1077C=	NP_001558.3:p.Phe359=
XM_005273978.3:c.1143C=	XP_005274035.1:p.Phe381=
XM_005273979.3:c.1143C=	XP_005274036.1:p.Phe381=
XM_011544999.1:c.1077C=	XP_011543301.1:p.Phe359=
XM_011545000.1:c.1143C=	XP_011543302.1:p.Phe381=
XM_005273979.4:c.1143C=	XP_005274036.1:p.Phe381=
XM_011544999.2:c.1077C=	XP_011543301.1:p.Phe359=
XM_024448501.1:c.1143C=	XP_024304269.1:p.Phe381=
XM_024448502.1:c.1143C=	XP_024304270.1:p.Phe381=
XM_024448503.1:c.1113C=	XP_024304271.1:p.Phe371=
XM_024448504.1:c.1077C=	XP_024304272.1:p.Phe359=
XM_024448505.1:c.1143C=	XP_024304273.1:p.Phe381=
NM_001567.4:c.1077C= MANE Select	NP_001558.3:p.Phe359=