Canonical Allele Identifier: CA1981895455

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225123C= , CM000673.2:g.72225123C=	GRCh38
NC_000011.9:g.71936167C= , CM000673.1:g.71936167C=	GRCh37
NC_000011.8:g.71613815C=	NCBI36
NG_023253.1:g.5286C=
NG_023253.2:g.5286C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.139C= MANE Select	ENSP00000298229.2:p.Arg47=
ENST00000298229.6:c.139C=	ENSP00000298229.2:p.Arg47=
ENST00000541544.1:n.55C=
NM_001567.3:c.139C=	NP_001558.3:p.Arg47=
XM_005273978.3:c.139C=	XP_005274035.1:p.Arg47=
XM_005273979.3:c.139C=	XP_005274036.1:p.Arg47=
XM_011544999.1:c.139C=	XP_011543301.1:p.Arg47=
XM_011545000.1:c.139C=	XP_011543302.1:p.Arg47=
XM_005273979.4:c.139C=	XP_005274036.1:p.Arg47=
XM_011544999.2:c.139C=	XP_011543301.1:p.Arg47=
XM_024448501.1:c.139C=	XP_024304269.1:p.Arg47=
XM_024448502.1:c.139C=	XP_024304270.1:p.Arg47=
XM_024448503.1:c.18C=	XP_024304271.1:p.Ser6=
XM_024448504.1:c.139C=	XP_024304272.1:p.Arg47=
XM_024448505.1:c.139C=	XP_024304273.1:p.Arg47=
NM_001567.4:c.139C= MANE Select	NP_001558.3:p.Arg47=