Canonical Allele Identifier: CA224375300

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72228854C>A , CM000673.2:g.72228854C>A	GRCh38
NC_000011.9:g.71939898C>A , CM000673.1:g.71939898C>A	GRCh37
NC_000011.8:g.71617546C>A	NCBI36
NG_023253.1:g.9017C>A
NG_023253.2:g.9017C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.518+7C>A MANE Select	ENSP00000298229.2:n.518+7C>A
ENST00000298229.6:c.518+7C>A	ENSP00000298229.2:n.518+7C>A
ENST00000537656.1:c.-444C>A	ENSP00000444630.1:n.-444C>A
ENST00000538751.5:c.-209+7C>A	ENSP00000444619.1:n.-209+7C>A
ENST00000540329.5:c.-209+7C>A	ENSP00000440018.1:n.-209+7C>A
ENST00000541756.5:c.320+7C>A	ENSP00000446360.2:n.320+7C>A
NM_001567.3:c.518+7C>A	NP_001558.3:n.518+7C>A
XM_005273978.3:c.518+7C>A	XP_005274035.1:n.518+7C>A
XM_005273979.3:c.518+7C>A	XP_005274036.1:n.518+7C>A
XM_011544999.1:c.518+7C>A	XP_011543301.1:n.518+7C>A
XM_011545000.1:c.518+7C>A	XP_011543302.1:n.518+7C>A
XM_005273979.4:c.518+7C>A	XP_005274036.1:n.518+7C>A
XM_011544999.2:c.518+7C>A	XP_011543301.1:n.518+7C>A
XM_024448501.1:c.518+7C>A	XP_024304269.1:n.518+7C>A
XM_024448502.1:c.518+7C>A	XP_024304270.1:n.518+7C>A
XM_024448503.1:c.488+7C>A	XP_024304271.1:n.488+7C>A
XM_024448504.1:c.518+7C>A	XP_024304272.1:n.518+7C>A
XM_024448505.1:c.518+7C>A	XP_024304273.1:n.518+7C>A
NM_001567.4:c.518+7C>A MANE Select	NP_001558.3:n.518+7C>A