Canonical Allele Identifier: CA1981895430

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225070_72225098delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG , CM000673.2:g.72225070_72225098delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	GRCh38
NC_000011.9:g.71936114_71936142delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG , CM000673.1:g.71936114_71936142delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	GRCh37
NC_000011.8:g.71613762_71613790delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	NCBI36
NG_023253.1:g.5233_5261delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG
NG_023253.2:g.5233_5261delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG MANE Select	ENSP00000298229.2:p.Ala29=
ENST00000298229.6:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	ENSP00000298229.2:p.Ala29=
ENST00000541544.1:n.2_30delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG
NM_001567.3:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	NP_001558.3:p.Ala29=
XM_005273978.3:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_005274035.1:p.Ala29=
XM_005273979.3:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_005274036.1:p.Ala29=
XM_011544999.1:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_011543301.1:p.Ala29=
XM_011545000.1:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_011543302.1:p.Ala29=
XM_005273979.4:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_005274036.1:p.Ala29=
XM_011544999.2:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_011543301.1:p.Ala29=
XM_024448501.1:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_024304269.1:p.Ala29=
XM_024448502.1:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_024304270.1:p.Ala29=
XM_024448503.1:c.-36_-8delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_024304271.1:n.-36_-8delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG
XM_024448504.1:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_024304272.1:p.Ala29=
XM_024448505.1:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG	XP_024304273.1:p.Ala29=
NM_001567.4:c.86_114delinsCGGCCGCGGAGGAGCTGCTGGCCCGGGCG MANE Select	NP_001558.3:p.Ala29=