Canonical Allele Identifier: CA918911913

Gene: INPPL1

Linked Data

• dbSNP Id: rs1591265588

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224698_72224707del , CM000673.2:g.72224698_72224707del	GRCh38
NC_000011.9:g.71935742_71935751del , CM000673.1:g.71935742_71935751del	GRCh37
NC_000011.8:g.71613390_71613399del	NCBI36
NG_023253.1:g.4861_4870del
NG_023253.2:g.4861_4870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540973.1:c.-205-82_-205-73del	ENSP00000440904.1:n.-205-82_-205-73del
ENST00000543234.1:c.-205-82_-205-73del	ENSP00000440512.1:n.-205-82_-205-73del
XM_005273978.3:c.-205-82_-205-73del	XP_005274035.1:n.-205-82_-205-73del
XM_005273979.3:c.-205-82_-205-73del	XP_005274036.1:n.-205-82_-205-73del
XM_011544999.1:c.-205-82_-205-73del	XP_011543301.1:n.-205-82_-205-73del
XM_011545000.1:c.-205-82_-205-73del	XP_011543302.1:n.-205-82_-205-73del
XM_005273979.4:c.-205-82_-205-73del	XP_005274036.1:n.-205-82_-205-73del
XM_011544999.2:c.-205-82_-205-73del	XP_011543301.1:n.-205-82_-205-73del
XM_024448501.1:c.-205-82_-205-73del	XP_024304269.1:n.-205-82_-205-73del
XM_024448502.1:c.-205-82_-205-73del	XP_024304270.1:n.-205-82_-205-73del
XM_024448503.1:c.-326-82_-326-73del	XP_024304271.1:n.-326-82_-326-73del
XM_024448504.1:c.-205-82_-205-73del	XP_024304272.1:n.-205-82_-205-73del
XM_024448505.1:c.-205-82_-205-73del	XP_024304273.1:n.-205-82_-205-73del