Canonical Allele Identifier: CA6169831

Gene: INPPL1

Linked Data

• dbSNP Id: rs765034075
• ExAC: 11:71941037 A / AC
• gnomAD v2: 11-71941037-A-AC
• MyVariant Identifiers: chr11:g.71941037_71941038insC (hg19) ; chr11:g.72229993_72229994insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229993_72229994insC , CM000673.2:g.72229993_72229994insC	GRCh38
NC_000011.9:g.71941037_71941038insC , CM000673.1:g.71941037_71941038insC	GRCh37
NC_000011.8:g.71618685_71618686insC	NCBI36
NG_023253.1:g.10156_10157insC
NG_023253.2:g.10156_10157insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.913_914insC MANE Select	ENSP00000298229.2:p.Lys305ThrfsTer9
ENST00000298229.6:c.913_914insC	ENSP00000298229.2:p.Lys305ThrfsTer9
ENST00000538751.5:c.187_188insC	ENSP00000444619.1:p.Lys63ThrfsTer9
ENST00000540329.5:c.97_98insC	ENSP00000440018.1:p.Lys33ThrfsTer9
ENST00000541756.5:c.715_716insC	ENSP00000446360.2:p.Lys239ThrfsTer9
NM_001567.3:c.913_914insC	NP_001558.3:p.Lys305ThrfsTer9
XM_005273978.3:c.979_980insC	XP_005274035.1:p.Lys327ThrfsTer9
XM_005273979.3:c.979_980insC	XP_005274036.1:p.Lys327ThrfsTer9
XM_011544999.1:c.913_914insC	XP_011543301.1:p.Lys305ThrfsTer9
XM_011545000.1:c.979_980insC	XP_011543302.1:p.Lys327ThrfsTer9
XM_005273979.4:c.979_980insC	XP_005274036.1:p.Lys327ThrfsTer9
XM_011544999.2:c.913_914insC	XP_011543301.1:p.Lys305ThrfsTer9
XM_024448501.1:c.979_980insC	XP_024304269.1:p.Lys327ThrfsTer9
XM_024448502.1:c.979_980insC	XP_024304270.1:p.Lys327ThrfsTer9
XM_024448503.1:c.949_950insC	XP_024304271.1:p.Lys317ThrfsTer9
XM_024448504.1:c.913_914insC	XP_024304272.1:p.Lys305ThrfsTer9
XM_024448505.1:c.979_980insC	XP_024304273.1:p.Lys327ThrfsTer9
NM_001567.4:c.913_914insC MANE Select	NP_001558.3:p.Lys305ThrfsTer9