Canonical Allele Identifier: CA1981895449

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225107T= , CM000673.2:g.72225107T=	GRCh38
NC_000011.9:g.71936151T= , CM000673.1:g.71936151T=	GRCh37
NC_000011.8:g.71613799T=	NCBI36
NG_023253.1:g.5270T=
NG_023253.2:g.5270T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.123T= MANE Select	ENSP00000298229.2:p.Asp41=
ENST00000298229.6:c.123T=	ENSP00000298229.2:p.Asp41=
ENST00000541544.1:n.39T=
NM_001567.3:c.123T=	NP_001558.3:p.Asp41=
XM_005273978.3:c.123T=	XP_005274035.1:p.Asp41=
XM_005273979.3:c.123T=	XP_005274036.1:p.Asp41=
XM_011544999.1:c.123T=	XP_011543301.1:p.Asp41=
XM_011545000.1:c.123T=	XP_011543302.1:p.Asp41=
XM_005273979.4:c.123T=	XP_005274036.1:p.Asp41=
XM_011544999.2:c.123T=	XP_011543301.1:p.Asp41=
XM_024448501.1:c.123T=	XP_024304269.1:p.Asp41=
XM_024448502.1:c.123T=	XP_024304270.1:p.Asp41=
XM_024448503.1:c.2T=	XP_024304271.1:p.Met1=
XM_024448504.1:c.123T=	XP_024304272.1:p.Asp41=
XM_024448505.1:c.123T=	XP_024304273.1:p.Asp41=
NM_001567.4:c.123T= MANE Select	NP_001558.3:p.Asp41=