Canonical Allele Identifier: CA679972443

Gene: INPPL1

Linked Data

• dbSNP Id: rs1312514992
• gnomAD v3: 11-72224719-C-CCTGCG
• gnomAD v4: 11-72224719-C-CCTGCG
• MyVariant Identifiers: chr11:g.71935763_71935764insCTGCG (hg19) ; chr11:g.72224719_72224720insCTGCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224722_72224726dup , CM000673.2:g.72224722_72224726dup	GRCh38
NC_000011.9:g.71935766_71935770dup , CM000673.1:g.71935766_71935770dup	GRCh37
NC_000011.8:g.71613414_71613418dup	NCBI36
NG_023253.1:g.4885_4889dup
NG_023253.2:g.4885_4889dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540973.1:c.-205-58_-205-54dup	ENSP00000440904.1:n.-205-58_-205-54dup
ENST00000543234.1:c.-205-58_-205-54dup	ENSP00000440512.1:n.-205-58_-205-54dup
XM_005273978.3:c.-205-58_-205-54dup	XP_005274035.1:n.-205-58_-205-54dup
XM_005273979.3:c.-205-58_-205-54dup	XP_005274036.1:n.-205-58_-205-54dup
XM_011544999.1:c.-205-58_-205-54dup	XP_011543301.1:n.-205-58_-205-54dup
XM_011545000.1:c.-205-58_-205-54dup	XP_011543302.1:n.-205-58_-205-54dup
XM_005273979.4:c.-205-58_-205-54dup	XP_005274036.1:n.-205-58_-205-54dup
XM_011544999.2:c.-205-58_-205-54dup	XP_011543301.1:n.-205-58_-205-54dup
XM_024448501.1:c.-205-58_-205-54dup	XP_024304269.1:n.-205-58_-205-54dup
XM_024448502.1:c.-205-58_-205-54dup	XP_024304270.1:n.-205-58_-205-54dup
XM_024448503.1:c.-326-58_-326-54dup	XP_024304271.1:n.-326-58_-326-54dup
XM_024448504.1:c.-205-58_-205-54dup	XP_024304272.1:n.-205-58_-205-54dup
XM_024448505.1:c.-205-58_-205-54dup	XP_024304273.1:n.-205-58_-205-54dup