Canonical Allele Identifier: CA1981895283

Gene: INPPL1

Linked Data

• dbSNP Id: rs1948620594

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224816_72224836del , CM000673.2:g.72224816_72224836del	GRCh38
NC_000011.9:g.71935860_71935880del , CM000673.1:g.71935860_71935880del	GRCh37
NC_000011.8:g.71613508_71613528del	NCBI36
NG_023253.1:g.4979_4999del
NG_023253.2:g.4979_4999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.-169_-149del MANE Select	ENSP00000298229.2:n.-169_-149del
ENST00000298229.6:c.-169_-149del	ENSP00000298229.2:n.-169_-149del
ENST00000540973.1:c.-169_-149del	ENSP00000440904.1:n.-169_-149del
ENST00000543234.1:c.-169_-149del	ENSP00000440512.1:n.-169_-149del
XM_005273978.3:c.-169_-149del	XP_005274035.1:n.-169_-149del
XM_005273979.3:c.-169_-149del	XP_005274036.1:n.-169_-149del
XM_011544999.1:c.-169_-149del	XP_011543301.1:n.-169_-149del
XM_011545000.1:c.-169_-149del	XP_011543302.1:n.-169_-149del
XM_005273979.4:c.-169_-149del	XP_005274036.1:n.-169_-149del
XM_011544999.2:c.-169_-149del	XP_011543301.1:n.-169_-149del
XM_024448501.1:c.-169_-149del	XP_024304269.1:n.-169_-149del
XM_024448502.1:c.-169_-149del	XP_024304270.1:n.-169_-149del
XM_024448503.1:c.-290_-270del	XP_024304271.1:n.-290_-270del
XM_024448504.1:c.-169_-149del	XP_024304272.1:n.-169_-149del
XM_024448505.1:c.-169_-149del	XP_024304273.1:n.-169_-149del
NM_001567.4:c.-169_-149del MANE Select	NP_001558.3:n.-169_-149del