Canonical Allele Identifier: CA2536750968

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230627_72230631del , CM000673.2:g.72230627_72230631del	GRCh38
NC_000011.9:g.71941671_71941675del , CM000673.1:g.71941671_71941675del	GRCh37
NC_000011.8:g.71619319_71619323del	NCBI36
NG_023253.1:g.10790_10794del
NG_023253.2:g.10790_10794del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1197+159_1197+163del MANE Select	ENSP00000298229.2:n.1197+159_1197+163del
ENST00000298229.6:c.1197+159_1197+163del	ENSP00000298229.2:n.1197+159_1197+163del
ENST00000538751.5:c.471+159_471+163del	ENSP00000444619.1:n.471+159_471+163del
ENST00000541756.5:c.999+159_999+163del	ENSP00000446360.2:n.999+159_999+163del
NM_001567.3:c.1197+159_1197+163del	NP_001558.3:n.1197+159_1197+163del
XM_005273978.3:c.1263+159_1263+163del	XP_005274035.1:n.1263+159_1263+163del
XM_005273979.3:c.1263+159_1263+163del	XP_005274036.1:n.1263+159_1263+163del
XM_011544999.1:c.1197+159_1197+163del	XP_011543301.1:n.1197+159_1197+163del
XM_011545000.1:c.1263+159_1263+163del	XP_011543302.1:n.1263+159_1263+163del
XM_005273979.4:c.1263+159_1263+163del	XP_005274036.1:n.1263+159_1263+163del
XM_011544999.2:c.1197+159_1197+163del	XP_011543301.1:n.1197+159_1197+163del
XM_024448501.1:c.1263+159_1263+163del	XP_024304269.1:n.1263+159_1263+163del
XM_024448502.1:c.1263+159_1263+163del	XP_024304270.1:n.1263+159_1263+163del
XM_024448503.1:c.1233+159_1233+163del	XP_024304271.1:n.1233+159_1233+163del
XM_024448504.1:c.1197+159_1197+163del	XP_024304272.1:n.1197+159_1197+163del
XM_024448505.1:c.1263+159_1263+163del	XP_024304273.1:n.1263+159_1263+163del
NM_001567.4:c.1197+159_1197+163del MANE Select	NP_001558.3:n.1197+159_1197+163del