Canonical Allele Identifier: CA1981895446

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225100G= , CM000673.2:g.72225100G=	GRCh38
NC_000011.9:g.71936144G= , CM000673.1:g.71936144G=	GRCh37
NC_000011.8:g.71613792G=	NCBI36
NG_023253.1:g.5263G=
NG_023253.2:g.5263G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.116G= MANE Select	ENSP00000298229.2:p.Gly39=
ENST00000298229.6:c.116G=	ENSP00000298229.2:p.Gly39=
ENST00000541544.1:n.32G=
NM_001567.3:c.116G=	NP_001558.3:p.Gly39=
XM_005273978.3:c.116G=	XP_005274035.1:p.Gly39=
XM_005273979.3:c.116G=	XP_005274036.1:p.Gly39=
XM_011544999.1:c.116G=	XP_011543301.1:p.Gly39=
XM_011545000.1:c.116G=	XP_011543302.1:p.Gly39=
XM_005273979.4:c.116G=	XP_005274036.1:p.Gly39=
XM_011544999.2:c.116G=	XP_011543301.1:p.Gly39=
XM_024448501.1:c.116G=	XP_024304269.1:p.Gly39=
XM_024448502.1:c.116G=	XP_024304270.1:p.Gly39=
XM_024448503.1:c.-6G=	XP_024304271.1:n.-6G=
XM_024448504.1:c.116G=	XP_024304272.1:p.Gly39=
XM_024448505.1:c.116G=	XP_024304273.1:p.Gly39=
NM_001567.4:c.116G= MANE Select	NP_001558.3:p.Gly39=