Canonical Allele Identifier: CA224376091

Gene: INPPL1

Linked Data

• dbSNP Id: rs551020640
• gnomAD v2: 11-71941662-C-CG
• gnomAD v3: 11-72230618-C-CG
• gnomAD v4: 11-72230618-C-CG
• MyVariant Identifiers: chr11:g.71941663_71941664insG (hg19) ; chr11:g.71941662_71941663insG (hg19) ; chr11:g.72230619_72230620insG (hg38) ; chr11:g.72230618_72230619insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230621dup , CM000673.2:g.72230621dup	GRCh38
NC_000011.9:g.71941665dup , CM000673.1:g.71941665dup	GRCh37
NC_000011.8:g.71619313dup	NCBI36
NG_023253.1:g.10784dup
NG_023253.2:g.10784dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1197+153dup MANE Select	ENSP00000298229.2:n.1197+153dup
ENST00000298229.6:c.1197+153dup	ENSP00000298229.2:n.1197+153dup
ENST00000538751.5:c.471+153dup	ENSP00000444619.1:n.471+153dup
ENST00000541756.5:c.999+153dup	ENSP00000446360.2:n.999+153dup
NM_001567.3:c.1197+153dup	NP_001558.3:n.1197+153dup
XM_005273978.3:c.1263+153dup	XP_005274035.1:n.1263+153dup
XM_005273979.3:c.1263+153dup	XP_005274036.1:n.1263+153dup
XM_011544999.1:c.1197+153dup	XP_011543301.1:n.1197+153dup
XM_011545000.1:c.1263+153dup	XP_011543302.1:n.1263+153dup
XM_005273979.4:c.1263+153dup	XP_005274036.1:n.1263+153dup
XM_011544999.2:c.1197+153dup	XP_011543301.1:n.1197+153dup
XM_024448501.1:c.1263+153dup	XP_024304269.1:n.1263+153dup
XM_024448502.1:c.1263+153dup	XP_024304270.1:n.1263+153dup
XM_024448503.1:c.1233+153dup	XP_024304271.1:n.1233+153dup
XM_024448504.1:c.1197+153dup	XP_024304272.1:n.1197+153dup
XM_024448505.1:c.1263+153dup	XP_024304273.1:n.1263+153dup
NM_001567.4:c.1197+153dup MANE Select	NP_001558.3:n.1197+153dup