Canonical Allele Identifier: CA1981895433

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225074C= , CM000673.2:g.72225074C=	GRCh38
NC_000011.9:g.71936118C= , CM000673.1:g.71936118C=	GRCh37
NC_000011.8:g.71613766C=	NCBI36
NG_023253.1:g.5237C=
NG_023253.2:g.5237C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.90C= MANE Select	ENSP00000298229.2:p.Ala30=
ENST00000298229.6:c.90C=	ENSP00000298229.2:p.Ala30=
ENST00000541544.1:n.6C=
NM_001567.3:c.90C=	NP_001558.3:p.Ala30=
XM_005273978.3:c.90C=	XP_005274035.1:p.Ala30=
XM_005273979.3:c.90C=	XP_005274036.1:p.Ala30=
XM_011544999.1:c.90C=	XP_011543301.1:p.Ala30=
XM_011545000.1:c.90C=	XP_011543302.1:p.Ala30=
XM_005273979.4:c.90C=	XP_005274036.1:p.Ala30=
XM_011544999.2:c.90C=	XP_011543301.1:p.Ala30=
XM_024448501.1:c.90C=	XP_024304269.1:p.Ala30=
XM_024448502.1:c.90C=	XP_024304270.1:p.Ala30=
XM_024448503.1:c.-32C=	XP_024304271.1:n.-32C=
XM_024448504.1:c.90C=	XP_024304272.1:p.Ala30=
XM_024448505.1:c.90C=	XP_024304273.1:p.Ala30=
NM_001567.4:c.90C= MANE Select	NP_001558.3:p.Ala30=