Canonical Allele Identifier: CA224381000

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72236225G>A , CM000673.2:g.72236225G>A	GRCh38
NC_000011.9:g.71947269G>A , CM000673.1:g.71947269G>A	GRCh37
NC_000011.8:g.71624917G>A	NCBI36
NG_023253.1:g.16388G>A
NG_023253.2:g.16388G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.2879+239G>A MANE Select	ENSP00000298229.2:n.2879+239G>A
ENST00000298229.6:c.2879+239G>A	ENSP00000298229.2:n.2879+239G>A
ENST00000535985.1:c.268+1610G>A
ENST00000538751.5:c.2153+239G>A	ENSP00000444619.1:n.2153+239G>A
ENST00000541756.5:c.2681+239G>A	ENSP00000446360.2:n.2681+239G>A
NM_001567.3:c.2879+239G>A	NP_001558.3:n.2879+239G>A
XM_005273978.3:c.2945+239G>A	XP_005274035.1:n.2945+239G>A
XM_005273979.3:c.2945+239G>A	XP_005274036.1:n.2945+239G>A
XM_011544999.1:c.2879+239G>A	XP_011543301.1:n.2879+239G>A
XM_011545000.1:c.2945+239G>A	XP_011543302.1:n.2945+239G>A
XM_005273979.4:c.2945+239G>A	XP_005274036.1:n.2945+239G>A
XM_011544999.2:c.2879+239G>A	XP_011543301.1:n.2879+239G>A
XM_024448501.1:c.3077+239G>A	XP_024304269.1:n.3077+239G>A
XM_024448502.1:c.3077+239G>A	XP_024304270.1:n.3077+239G>A
XM_024448503.1:c.3047+239G>A	XP_024304271.1:n.3047+239G>A
XM_024448504.1:c.3011+239G>A	XP_024304272.1:n.3011+239G>A
XM_024448505.1:c.3077+239G>A	XP_024304273.1:n.3077+239G>A
NM_001567.4:c.2879+239G>A MANE Select	NP_001558.3:n.2879+239G>A