Canonical Allele Identifier: CA1981897899

Gene: INPPL1

Linked Data

• dbSNP Id: rs1948787881

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230063T>G , CM000673.2:g.72230063T>G	GRCh38
NC_000011.9:g.71941107T>G , CM000673.1:g.71941107T>G	GRCh37
NC_000011.8:g.71618755T>G	NCBI36
NG_023253.1:g.10226T>G
NG_023253.2:g.10226T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.939+44T>G MANE Select	ENSP00000298229.2:n.939+44T>G
ENST00000298229.6:c.939+44T>G	ENSP00000298229.2:n.939+44T>G
ENST00000538751.5:c.213+44T>G	ENSP00000444619.1:n.213+44T>G
ENST00000540329.5:c.123+44T>G	ENSP00000440018.1:n.123+44T>G
ENST00000541756.5:c.741+44T>G	ENSP00000446360.2:n.741+44T>G
NM_001567.3:c.939+44T>G	NP_001558.3:n.939+44T>G
XM_005273978.3:c.1005+44T>G	XP_005274035.1:n.1005+44T>G
XM_005273979.3:c.1005+44T>G	XP_005274036.1:n.1005+44T>G
XM_011544999.1:c.939+44T>G	XP_011543301.1:n.939+44T>G
XM_011545000.1:c.1005+44T>G	XP_011543302.1:n.1005+44T>G
XM_005273979.4:c.1005+44T>G	XP_005274036.1:n.1005+44T>G
XM_011544999.2:c.939+44T>G	XP_011543301.1:n.939+44T>G
XM_024448501.1:c.1005+44T>G	XP_024304269.1:n.1005+44T>G
XM_024448502.1:c.1005+44T>G	XP_024304270.1:n.1005+44T>G
XM_024448503.1:c.975+44T>G	XP_024304271.1:n.975+44T>G
XM_024448504.1:c.939+44T>G	XP_024304272.1:n.939+44T>G
XM_024448505.1:c.1005+44T>G	XP_024304273.1:n.1005+44T>G
NM_001567.4:c.939+44T>G MANE Select	NP_001558.3:n.939+44T>G