Canonical Allele Identifier: CA6169733

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229251del , CM000673.2:g.72229251del	GRCh38
NC_000011.9:g.71940295del , CM000673.1:g.71940295del	GRCh37
NC_000011.8:g.71617943del	NCBI36
NG_023253.1:g.9414del
NG_023253.2:g.9414del

Transcript Alleles

HGVS	Amino-acid Change
NM_001567.4:c.659+21del MANE Select	NP_001558.3:n.659+21del
ENST00000298229.7:c.659+21del MANE Select	ENSP00000298229.2:n.659+21del
NM_001567.3:c.659+21del	NP_001558.3:n.659+21del
ENST00000298229.6:c.659+21del	ENSP00000298229.2:n.659+21del
ENST00000537656.1:c.-68+21del	ENSP00000444630.1:n.-68+21del
ENST00000538751.5:c.-68+21del	ENSP00000444619.1:n.-68+21del
ENST00000540329.5:c.-68+21del	ENSP00000440018.1:n.-68+21del
ENST00000541756.5:c.461+21del	ENSP00000446360.2:n.461+21del
XM_005273978.3:c.725+21del	XP_005274035.1:n.725+21del
XM_005273979.3:c.725+21del	XP_005274036.1:n.725+21del
XM_005273979.4:c.725+21del	XP_005274036.1:n.725+21del
XM_011544999.1:c.659+21del	XP_011543301.1:n.659+21del
XM_011544999.2:c.659+21del	XP_011543301.1:n.659+21del
XM_011545000.1:c.725+21del	XP_011543302.1:n.725+21del
XM_024448501.1:c.725+21del	XP_024304269.1:n.725+21del
XM_024448502.1:c.725+21del	XP_024304270.1:n.725+21del
XM_024448503.1:c.695+21del	XP_024304271.1:n.695+21del
XM_024448504.1:c.659+21del	XP_024304272.1:n.659+21del
XM_024448505.1:c.725+21del	XP_024304273.1:n.725+21del