Canonical Allele Identifier: CA2552044101

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225331_72225338del , CM000673.2:g.72225331_72225338del	GRCh38
NC_000011.9:g.71936375_71936382del , CM000673.1:g.71936375_71936382del	GRCh37
NC_000011.8:g.71614023_71614030del	NCBI36
NG_023253.1:g.5494_5501del
NG_023253.2:g.5494_5501del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+165_182+172del MANE Select	ENSP00000298229.2:n.182+165_182+172del
ENST00000298229.6:c.182+165_182+172del	ENSP00000298229.2:n.182+165_182+172del
ENST00000541544.1:n.98+165_98+172del
NM_001567.3:c.182+165_182+172del	NP_001558.3:n.182+165_182+172del
XM_005273978.3:c.182+165_182+172del	XP_005274035.1:n.182+165_182+172del
XM_005273979.3:c.182+165_182+172del	XP_005274036.1:n.182+165_182+172del
XM_011544999.1:c.182+165_182+172del	XP_011543301.1:n.182+165_182+172del
XM_011545000.1:c.182+165_182+172del	XP_011543302.1:n.182+165_182+172del
XM_005273979.4:c.182+165_182+172del	XP_005274036.1:n.182+165_182+172del
XM_011544999.2:c.182+165_182+172del	XP_011543301.1:n.182+165_182+172del
XM_024448501.1:c.182+165_182+172del	XP_024304269.1:n.182+165_182+172del
XM_024448502.1:c.182+165_182+172del	XP_024304270.1:n.182+165_182+172del
XM_024448503.1:c.62-119_62-112del	XP_024304271.1:n.62-119_62-112del
XM_024448504.1:c.182+165_182+172del	XP_024304272.1:n.182+165_182+172del
XM_024448505.1:c.182+165_182+172del	XP_024304273.1:n.182+165_182+172del
NM_001567.4:c.182+165_182+172del MANE Select	NP_001558.3:n.182+165_182+172del