Canonical Allele Identifier: CA1981895459

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225138G= , CM000673.2:g.72225138G=	GRCh38
NC_000011.9:g.71936182G= , CM000673.1:g.71936182G=	GRCh37
NC_000011.8:g.71613830G=	NCBI36
NG_023253.1:g.5301G=
NG_023253.2:g.5301G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.154G= MANE Select	ENSP00000298229.2:p.Val52=
ENST00000298229.6:c.154G=	ENSP00000298229.2:p.Val52=
ENST00000541544.1:n.70G=
NM_001567.3:c.154G=	NP_001558.3:p.Val52=
XM_005273978.3:c.154G=	XP_005274035.1:p.Val52=
XM_005273979.3:c.154G=	XP_005274036.1:p.Val52=
XM_011544999.1:c.154G=	XP_011543301.1:p.Val52=
XM_011545000.1:c.154G=	XP_011543302.1:p.Val52=
XM_005273979.4:c.154G=	XP_005274036.1:p.Val52=
XM_011544999.2:c.154G=	XP_011543301.1:p.Val52=
XM_024448501.1:c.154G=	XP_024304269.1:p.Val52=
XM_024448502.1:c.154G=	XP_024304270.1:p.Val52=
XM_024448503.1:c.33G=	XP_024304271.1:p.Ala11=
XM_024448504.1:c.154G=	XP_024304272.1:p.Val52=
XM_024448505.1:c.154G=	XP_024304273.1:p.Val52=
NM_001567.4:c.154G= MANE Select	NP_001558.3:p.Val52=