Canonical Allele Identifier: CA381734381

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72234556C>T , CM000673.2:g.72234556C>T	GRCh38
NC_000011.9:g.71945600C>T , CM000673.1:g.71945600C>T	GRCh37
NC_000011.8:g.71623248C>T	NCBI36
NG_023253.1:g.14719C>T
NG_023253.2:g.14719C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001567.4:c.2356C>T MANE Select	NP_001558.3:p.Gln786Ter
ENST00000298229.7:c.2356C>T MANE Select	ENSP00000298229.2:p.Gln786Ter
NM_001567.3:c.2356C>T	NP_001558.3:p.Gln786Ter
ENST00000298229.6:c.2356C>T	ENSP00000298229.2:p.Gln786Ter
ENST00000535985.1:c.209C>T
ENST00000538751.5:c.1630C>T	ENSP00000444619.1:p.Gln544Ter
ENST00000541303.5:n.962C>T
ENST00000541756.5:c.2158C>T	ENSP00000446360.2:p.Gln720Ter
ENST00000545355.5:n.641C>T
XM_005273978.3:c.2422C>T	XP_005274035.1:p.Gln808Ter
XM_005273979.3:c.2422C>T	XP_005274036.1:p.Gln808Ter
XM_005273979.4:c.2422C>T	XP_005274036.1:p.Gln808Ter
XM_011544999.1:c.2356C>T	XP_011543301.1:p.Gln786Ter
XM_011544999.2:c.2356C>T	XP_011543301.1:p.Gln786Ter
XM_011545000.1:c.2422C>T	XP_011543302.1:p.Gln808Ter
XM_024448501.1:c.2554C>T	XP_024304269.1:p.Gln852Ter
XM_024448502.1:c.2554C>T	XP_024304270.1:p.Gln852Ter
XM_024448503.1:c.2524C>T	XP_024304271.1:p.Gln842Ter
XM_024448504.1:c.2488C>T	XP_024304272.1:p.Gln830Ter
XM_024448505.1:c.2554C>T	XP_024304273.1:p.Gln852Ter