Canonical Allele Identifier: CA1981899640

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72233696T= , CM000673.2:g.72233696T=	GRCh38
NC_000011.9:g.71944740T= , CM000673.1:g.71944740T=	GRCh37
NC_000011.8:g.71622388T=	NCBI36
NG_023253.1:g.13859T=
NG_023253.2:g.13859T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001567.4:c.2164T= MANE Select	NP_001558.3:p.Phe722=
ENST00000298229.7:c.2164T= MANE Select	ENSP00000298229.2:p.Phe722=
NM_001567.3:c.2164T=	NP_001558.3:p.Phe722=
ENST00000298229.6:c.2164T=	ENSP00000298229.2:p.Phe722=
ENST00000535985.1:c.17T=
ENST00000538751.5:c.1438T=	ENSP00000444619.1:p.Phe480=
ENST00000541303.5:n.770T=
ENST00000541756.5:c.1966T=	ENSP00000446360.2:p.Phe656=
ENST00000545355.5:n.449T=
XM_005273978.3:c.2230T=	XP_005274035.1:p.Phe744=
XM_005273979.3:c.2230T=	XP_005274036.1:p.Phe744=
XM_005273979.4:c.2230T=	XP_005274036.1:p.Phe744=
XM_011544999.1:c.2164T=	XP_011543301.1:p.Phe722=
XM_011544999.2:c.2164T=	XP_011543301.1:p.Phe722=
XM_011545000.1:c.2230T=	XP_011543302.1:p.Phe744=
XM_024448501.1:c.2362T=	XP_024304269.1:p.Phe788=
XM_024448502.1:c.2362T=	XP_024304270.1:p.Phe788=
XM_024448503.1:c.2332T=	XP_024304271.1:p.Phe778=
XM_024448504.1:c.2296T=	XP_024304272.1:p.Phe766=
XM_024448505.1:c.2362T=	XP_024304273.1:p.Phe788=