Canonical Allele Identifier: CA1981898038

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230353A= , CM000673.2:g.72230353A=	GRCh38
NC_000011.9:g.71941397A= , CM000673.1:g.71941397A=	GRCh37
NC_000011.8:g.71619045A=	NCBI36
NG_023253.1:g.10516A=
NG_023253.2:g.10516A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298229.7:c.1091-9A= MANE Select	ENSP00000298229.2:n.1091-9A=
ENST00000298229.6:c.1091-9A=	ENSP00000298229.2:n.1091-9A=
ENST00000538751.5:c.365-9A=	ENSP00000444619.1:n.365-9A=
ENST00000540329.5:c.275-9A=	ENSP00000440018.1:n.275-9A=
ENST00000541756.5:c.893-9A=	ENSP00000446360.2:n.893-9A=
NM_001567.3:c.1091-9A=	NP_001558.3:n.1091-9A=
XM_005273978.3:c.1157-9A=	XP_005274035.1:n.1157-9A=
XM_005273979.3:c.1157-9A=	XP_005274036.1:n.1157-9A=
XM_011544999.1:c.1091-9A=	XP_011543301.1:n.1091-9A=
XM_011545000.1:c.1157-9A=	XP_011543302.1:n.1157-9A=
XM_005273979.4:c.1157-9A=	XP_005274036.1:n.1157-9A=
XM_011544999.2:c.1091-9A=	XP_011543301.1:n.1091-9A=
XM_024448501.1:c.1157-9A=	XP_024304269.1:n.1157-9A=
XM_024448502.1:c.1157-9A=	XP_024304270.1:n.1157-9A=
XM_024448503.1:c.1127-9A=	XP_024304271.1:n.1127-9A=
XM_024448504.1:c.1091-9A=	XP_024304272.1:n.1091-9A=
XM_024448505.1:c.1157-9A=	XP_024304273.1:n.1157-9A=
NM_001567.4:c.1091-9A= MANE Select	NP_001558.3:n.1091-9A=