Canonical Allele Identifier: CA1981897865

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229991C= , CM000673.2:g.72229991C=	GRCh38
NC_000011.9:g.71941035C= , CM000673.1:g.71941035C=	GRCh37
NC_000011.8:g.71618683C=	NCBI36
NG_023253.1:g.10154C=
NG_023253.2:g.10154C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.911C= MANE Select	ENSP00000298229.2:p.Ala304=
ENST00000298229.6:c.911C=	ENSP00000298229.2:p.Ala304=
ENST00000538751.5:c.185C=	ENSP00000444619.1:p.Ala62=
ENST00000540329.5:c.95C=	ENSP00000440018.1:p.Ala32=
ENST00000541756.5:c.713C=	ENSP00000446360.2:p.Ala238=
NM_001567.3:c.911C=	NP_001558.3:p.Ala304=
XM_005273978.3:c.977C=	XP_005274035.1:p.Ala326=
XM_005273979.3:c.977C=	XP_005274036.1:p.Ala326=
XM_011544999.1:c.911C=	XP_011543301.1:p.Ala304=
XM_011545000.1:c.977C=	XP_011543302.1:p.Ala326=
XM_005273979.4:c.977C=	XP_005274036.1:p.Ala326=
XM_011544999.2:c.911C=	XP_011543301.1:p.Ala304=
XM_024448501.1:c.977C=	XP_024304269.1:p.Ala326=
XM_024448502.1:c.977C=	XP_024304270.1:p.Ala326=
XM_024448503.1:c.947C=	XP_024304271.1:p.Ala316=
XM_024448504.1:c.911C=	XP_024304272.1:p.Ala304=
XM_024448505.1:c.977C=	XP_024304273.1:p.Ala326=
NM_001567.4:c.911C= MANE Select	NP_001558.3:p.Ala304=