Canonical Allele Identifier: CA475866038

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71941284G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230240G>A , CM000673.2:g.72230240G>A	GRCh38
NC_000011.9:g.71941284G>A , CM000673.1:g.71941284G>A	GRCh37
NC_000011.8:g.71618932G>A	NCBI36
NG_023253.1:g.10403G>A
NG_023253.2:g.10403G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298229.7:c.1059G>A MANE Select	ENSP00000298229.2:p.Gln353=
ENST00000298229.6:c.1059G>A	ENSP00000298229.2:p.Gln353=
ENST00000538751.5:c.333G>A	ENSP00000444619.1:p.Gln111=
ENST00000540329.5:c.243G>A	ENSP00000440018.1:p.Gln81=
ENST00000541756.5:c.861G>A	ENSP00000446360.2:p.Gln287=
NM_001567.3:c.1059G>A	NP_001558.3:p.Gln353=
XM_005273978.3:c.1125G>A	XP_005274035.1:p.Gln375=
XM_005273979.3:c.1125G>A	XP_005274036.1:p.Gln375=
XM_011544999.1:c.1059G>A	XP_011543301.1:p.Gln353=
XM_011545000.1:c.1125G>A	XP_011543302.1:p.Gln375=
XM_005273979.4:c.1125G>A	XP_005274036.1:p.Gln375=
XM_011544999.2:c.1059G>A	XP_011543301.1:p.Gln353=
XM_024448501.1:c.1125G>A	XP_024304269.1:p.Gln375=
XM_024448502.1:c.1125G>A	XP_024304270.1:p.Gln375=
XM_024448503.1:c.1095G>A	XP_024304271.1:p.Gln365=
XM_024448504.1:c.1059G>A	XP_024304272.1:p.Gln353=
XM_024448505.1:c.1125G>A	XP_024304273.1:p.Gln375=
NM_001567.4:c.1059G>A MANE Select	NP_001558.3:p.Gln353=