Canonical Allele Identifier: CA679972927

Gene: INPPL1

Linked Data

• dbSNP Id: rs1489270333
• gnomAD v3: 11-72225203-A-AC
• gnomAD v4: 11-72225203-A-AC
• MyVariant Identifiers: chr11:g.71936247_71936248insC (hg19) ; chr11:g.72225203_72225204insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225205dup , CM000673.2:g.72225205dup	GRCh38
NC_000011.9:g.71936249dup , CM000673.1:g.71936249dup	GRCh37
NC_000011.8:g.71613897dup	NCBI36
NG_023253.1:g.5368dup
NG_023253.2:g.5368dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+39dup MANE Select	ENSP00000298229.2:n.182+39dup
ENST00000298229.6:c.182+39dup	ENSP00000298229.2:n.182+39dup
ENST00000541544.1:n.98+39dup
NM_001567.3:c.182+39dup	NP_001558.3:n.182+39dup
XM_005273978.3:c.182+39dup	XP_005274035.1:n.182+39dup
XM_005273979.3:c.182+39dup	XP_005274036.1:n.182+39dup
XM_011544999.1:c.182+39dup	XP_011543301.1:n.182+39dup
XM_011545000.1:c.182+39dup	XP_011543302.1:n.182+39dup
XM_005273979.4:c.182+39dup	XP_005274036.1:n.182+39dup
XM_011544999.2:c.182+39dup	XP_011543301.1:n.182+39dup
XM_024448501.1:c.182+39dup	XP_024304269.1:n.182+39dup
XM_024448502.1:c.182+39dup	XP_024304270.1:n.182+39dup
XM_024448503.1:c.61+39dup	XP_024304271.1:n.61+39dup
XM_024448504.1:c.182+39dup	XP_024304272.1:n.182+39dup
XM_024448505.1:c.182+39dup	XP_024304273.1:n.182+39dup
NM_001567.4:c.182+39dup MANE Select	NP_001558.3:n.182+39dup