Canonical Allele Identifier: CA2614950555

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72224804-G-GCGGCTGCGCGGTGAACGAGGCGGCCTGCAGCGC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224832_72224833insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC , CM000673.2:g.72224832_72224833insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	GRCh38
NC_000011.9:g.71935876_71935877insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC , CM000673.1:g.71935876_71935877insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	GRCh37
NC_000011.8:g.71613524_71613525insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	NCBI36
NG_023253.1:g.4995_4996insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC
NG_023253.2:g.4995_4996insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC MANE Select	ENSP00000298229.2:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGC...
ENST00000298229.6:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	ENSP00000298229.2:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGC...
ENST00000540973.1:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	ENSP00000440904.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGC...
ENST00000543234.1:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	ENSP00000440512.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGC...
XM_005273978.3:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_005274035.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_005273979.3:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_005274036.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_011544999.1:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_011543301.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_011545000.1:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_011543302.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_005273979.4:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_005274036.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_011544999.2:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_011543301.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_024448501.1:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_024304269.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_024448502.1:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_024304270.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_024448503.1:c.-274_-273insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_024304271.1:n.-274_-273insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_024448504.1:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_024304272.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
XM_024448505.1:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC	XP_024304273.1:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTG...
NM_001567.4:c.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC MANE Select	NP_001558.3:n.-153_-152insAGCGCCGGCTGCGCGGTGAACGAGGCGGCCTGC