Canonical Allele Identifier: CA2792650687

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230047_72230048del , CM000673.2:g.72230047_72230048del	GRCh38
NC_000011.9:g.71941091_71941092del , CM000673.1:g.71941091_71941092del	GRCh37
NC_000011.8:g.71618739_71618740del	NCBI36
NG_023253.1:g.10210_10211del
NG_023253.2:g.10210_10211del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.939+28_939+29del MANE Select	ENSP00000298229.2:n.939+28_939+29del
ENST00000298229.6:c.939+28_939+29del	ENSP00000298229.2:n.939+28_939+29del
ENST00000538751.5:c.213+28_213+29del	ENSP00000444619.1:n.213+28_213+29del
ENST00000540329.5:c.123+28_123+29del	ENSP00000440018.1:n.123+28_123+29del
ENST00000541756.5:c.741+28_741+29del	ENSP00000446360.2:n.741+28_741+29del
NM_001567.3:c.939+28_939+29del	NP_001558.3:n.939+28_939+29del
XM_005273978.3:c.1005+28_1005+29del	XP_005274035.1:n.1005+28_1005+29del
XM_005273979.3:c.1005+28_1005+29del	XP_005274036.1:n.1005+28_1005+29del
XM_011544999.1:c.939+28_939+29del	XP_011543301.1:n.939+28_939+29del
XM_011545000.1:c.1005+28_1005+29del	XP_011543302.1:n.1005+28_1005+29del
XM_005273979.4:c.1005+28_1005+29del	XP_005274036.1:n.1005+28_1005+29del
XM_011544999.2:c.939+28_939+29del	XP_011543301.1:n.939+28_939+29del
XM_024448501.1:c.1005+28_1005+29del	XP_024304269.1:n.1005+28_1005+29del
XM_024448502.1:c.1005+28_1005+29del	XP_024304270.1:n.1005+28_1005+29del
XM_024448503.1:c.975+28_975+29del	XP_024304271.1:n.975+28_975+29del
XM_024448504.1:c.939+28_939+29del	XP_024304272.1:n.939+28_939+29del
XM_024448505.1:c.1005+28_1005+29del	XP_024304273.1:n.1005+28_1005+29del
NM_001567.4:c.939+28_939+29del MANE Select	NP_001558.3:n.939+28_939+29del