Canonical Allele Identifier: CA1981895390

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224989_72224994delinsCCTCGG , CM000673.2:g.72224989_72224994delinsCCTCGG	GRCh38
NC_000011.9:g.71936033_71936038delinsCCTCGG , CM000673.1:g.71936033_71936038delinsCCTCGG	GRCh37
NC_000011.8:g.71613681_71613686delinsCCTCGG	NCBI36
NG_023253.1:g.5152_5157delinsCCTCGG
NG_023253.2:g.5152_5157delinsCCTCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.5_10delinsCCTCGG MANE Select	ENSP00000298229.2:p.Ala2=
ENST00000298229.6:c.5_10delinsCCTCGG	ENSP00000298229.2:p.Ala2=
ENST00000540973.1:c.5_10delinsCCTCGG	ENSP00000440904.1:p.Ala2=
ENST00000543234.1:c.5_10delinsCCTCGG	ENSP00000440512.1:p.Ala2=
NM_001567.3:c.5_10delinsCCTCGG	NP_001558.3:p.Ala2=
XM_005273978.3:c.5_10delinsCCTCGG	XP_005274035.1:p.Ala2=
XM_005273979.3:c.5_10delinsCCTCGG	XP_005274036.1:p.Ala2=
XM_011544999.1:c.5_10delinsCCTCGG	XP_011543301.1:p.Ala2=
XM_011545000.1:c.5_10delinsCCTCGG	XP_011543302.1:p.Ala2=
XM_005273979.4:c.5_10delinsCCTCGG	XP_005274036.1:p.Ala2=
XM_011544999.2:c.5_10delinsCCTCGG	XP_011543301.1:p.Ala2=
XM_024448501.1:c.5_10delinsCCTCGG	XP_024304269.1:p.Ala2=
XM_024448502.1:c.5_10delinsCCTCGG	XP_024304270.1:p.Ala2=
XM_024448503.1:c.-117_-112delinsCCTCGG	XP_024304271.1:n.-117_-112delinsCCTCGG
XM_024448504.1:c.5_10delinsCCTCGG	XP_024304272.1:p.Ala2=
XM_024448505.1:c.5_10delinsCCTCGG	XP_024304273.1:p.Ala2=
NM_001567.4:c.5_10delinsCCTCGG MANE Select	NP_001558.3:p.Ala2=