Canonical Allele Identifier: CA6169622

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72228434C>T , CM000673.2:g.72228434C>T	GRCh38
NC_000011.9:g.71939478C>T , CM000673.1:g.71939478C>T	GRCh37
NC_000011.8:g.71617126C>T	NCBI36
NG_023253.1:g.8597C>T
NG_023253.2:g.8597C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.333C>T MANE Select	ENSP00000298229.2:p.Cys111=
ENST00000298229.6:c.333C>T	ENSP00000298229.2:p.Cys111=
ENST00000538751.5:c.-394C>T	ENSP00000444619.1:n.-394C>T
ENST00000541544.1:n.249C>T
ENST00000541756.5:c.140C>T	ENSP00000446360.2:p.Ala47Val
NM_001567.3:c.333C>T	NP_001558.3:p.Cys111=
XM_005273978.3:c.333C>T	XP_005274035.1:p.Cys111=
XM_005273979.3:c.333C>T	XP_005274036.1:p.Cys111=
XM_011544999.1:c.333C>T	XP_011543301.1:p.Cys111=
XM_011545000.1:c.333C>T	XP_011543302.1:p.Cys111=
XM_005273979.4:c.333C>T	XP_005274036.1:p.Cys111=
XM_011544999.2:c.333C>T	XP_011543301.1:p.Cys111=
XM_024448501.1:c.333C>T	XP_024304269.1:p.Cys111=
XM_024448502.1:c.333C>T	XP_024304270.1:p.Cys111=
XM_024448503.1:c.303C>T	XP_024304271.1:p.Cys101=
XM_024448504.1:c.333C>T	XP_024304272.1:p.Cys111=
XM_024448505.1:c.333C>T	XP_024304273.1:p.Cys111=
NM_001567.4:c.333C>T MANE Select	NP_001558.3:p.Cys111=