Canonical Allele Identifier: CA679972477

Gene: INPPL1

Linked Data

• dbSNP Id: rs1421401396
• MyVariant Identifiers: chr11:g.71935849_71935850insGGCTGCGCGGTGAACGAGGCG (hg19) ; chr11:g.72224805_72224806insGGCTGCGCGGTGAACGAGGCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224807_72224827dup , CM000673.2:g.72224807_72224827dup	GRCh38
NC_000011.9:g.71935851_71935871dup , CM000673.1:g.71935851_71935871dup	GRCh37
NC_000011.8:g.71613499_71613519dup	NCBI36
NG_023253.1:g.4970_4990dup
NG_023253.2:g.4970_4990dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.-178_-158dup MANE Select	ENSP00000298229.2:n.-178_-158dup
ENST00000298229.6:c.-178_-158dup	ENSP00000298229.2:n.-178_-158dup
ENST00000540973.1:c.-178_-158dup	ENSP00000440904.1:n.-178_-158dup
ENST00000543234.1:c.-178_-158dup	ENSP00000440512.1:n.-178_-158dup
XM_005273978.3:c.-178_-158dup	XP_005274035.1:n.-178_-158dup
XM_005273979.3:c.-178_-158dup	XP_005274036.1:n.-178_-158dup
XM_011544999.1:c.-178_-158dup	XP_011543301.1:n.-178_-158dup
XM_011545000.1:c.-178_-158dup	XP_011543302.1:n.-178_-158dup
XM_005273979.4:c.-178_-158dup	XP_005274036.1:n.-178_-158dup
XM_011544999.2:c.-178_-158dup	XP_011543301.1:n.-178_-158dup
XM_024448501.1:c.-178_-158dup	XP_024304269.1:n.-178_-158dup
XM_024448502.1:c.-178_-158dup	XP_024304270.1:n.-178_-158dup
XM_024448503.1:c.-299_-279dup	XP_024304271.1:n.-299_-279dup
XM_024448504.1:c.-178_-158dup	XP_024304272.1:n.-178_-158dup
XM_024448505.1:c.-178_-158dup	XP_024304273.1:n.-178_-158dup
NM_001567.4:c.-178_-158dup MANE Select	NP_001558.3:n.-178_-158dup