Canonical Allele Identifier: CA1981898181

Gene: INPPL1

Linked Data

• dbSNP Id: rs1948807026
• gnomAD v3: 11-72230661-G-A
• gnomAD v4: 11-72230661-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230661G>A , CM000673.2:g.72230661G>A	GRCh38
NC_000011.9:g.71941705G>A , CM000673.1:g.71941705G>A	GRCh37
NC_000011.8:g.71619353G>A	NCBI36
NG_023253.1:g.10824G>A
NG_023253.2:g.10824G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1198-135G>A MANE Select	ENSP00000298229.2:n.1198-135G>A
ENST00000298229.6:c.1198-135G>A	ENSP00000298229.2:n.1198-135G>A
ENST00000538751.5:c.472-135G>A	ENSP00000444619.1:n.472-135G>A
ENST00000541756.5:c.1000-135G>A	ENSP00000446360.2:n.1000-135G>A
NM_001567.3:c.1198-135G>A	NP_001558.3:n.1198-135G>A
XM_005273978.3:c.1264-135G>A	XP_005274035.1:n.1264-135G>A
XM_005273979.3:c.1264-135G>A	XP_005274036.1:n.1264-135G>A
XM_011544999.1:c.1198-135G>A	XP_011543301.1:n.1198-135G>A
XM_011545000.1:c.1264-135G>A	XP_011543302.1:n.1264-135G>A
XM_005273979.4:c.1264-135G>A	XP_005274036.1:n.1264-135G>A
XM_011544999.2:c.1198-135G>A	XP_011543301.1:n.1198-135G>A
XM_024448501.1:c.1264-135G>A	XP_024304269.1:n.1264-135G>A
XM_024448502.1:c.1264-135G>A	XP_024304270.1:n.1264-135G>A
XM_024448503.1:c.1234-135G>A	XP_024304271.1:n.1234-135G>A
XM_024448504.1:c.1198-135G>A	XP_024304272.1:n.1198-135G>A
XM_024448505.1:c.1264-135G>A	XP_024304273.1:n.1264-135G>A
NM_001567.4:c.1198-135G>A MANE Select	NP_001558.3:n.1198-135G>A