Canonical Allele Identifier: CA1981897984

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230252C= , CM000673.2:g.72230252C=	GRCh38
NC_000011.9:g.71941296C= , CM000673.1:g.71941296C=	GRCh37
NC_000011.8:g.71618944C=	NCBI36
NG_023253.1:g.10415C=
NG_023253.2:g.10415C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1071C= MANE Select	ENSP00000298229.2:p.Thr357=
ENST00000298229.6:c.1071C=	ENSP00000298229.2:p.Thr357=
ENST00000538751.5:c.345C=	ENSP00000444619.1:p.Thr115=
ENST00000540329.5:c.255C=	ENSP00000440018.1:p.Thr85=
ENST00000541756.5:c.873C=	ENSP00000446360.2:p.Thr291=
NM_001567.3:c.1071C=	NP_001558.3:p.Thr357=
XM_005273978.3:c.1137C=	XP_005274035.1:p.Thr379=
XM_005273979.3:c.1137C=	XP_005274036.1:p.Thr379=
XM_011544999.1:c.1071C=	XP_011543301.1:p.Thr357=
XM_011545000.1:c.1137C=	XP_011543302.1:p.Thr379=
XM_005273979.4:c.1137C=	XP_005274036.1:p.Thr379=
XM_011544999.2:c.1071C=	XP_011543301.1:p.Thr357=
XM_024448501.1:c.1137C=	XP_024304269.1:p.Thr379=
XM_024448502.1:c.1137C=	XP_024304270.1:p.Thr379=
XM_024448503.1:c.1107C=	XP_024304271.1:p.Thr369=
XM_024448504.1:c.1071C=	XP_024304272.1:p.Thr357=
XM_024448505.1:c.1137C=	XP_024304273.1:p.Thr379=
NM_001567.4:c.1071C= MANE Select	NP_001558.3:p.Thr357=