Canonical Allele Identifier: CA1981897733

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229677A= , CM000673.2:g.72229677A=	GRCh38
NC_000011.9:g.71940721A= , CM000673.1:g.71940721A=	GRCh37
NC_000011.8:g.71618369A=	NCBI36
NG_023253.1:g.9840A=
NG_023253.2:g.9840A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001567.4:c.768A= MANE Select	NP_001558.3:p.Thr256=
ENST00000298229.7:c.768A= MANE Select	ENSP00000298229.2:p.Thr256=
NM_001567.3:c.768A=	NP_001558.3:p.Thr256=
ENST00000298229.6:c.768A=	ENSP00000298229.2:p.Thr256=
ENST00000537656.1:c.42A=	ENSP00000444630.1:p.Thr14=
ENST00000538751.5:c.42A=	ENSP00000444619.1:p.Thr14=
ENST00000540329.5:c.27+119A=	ENSP00000440018.1:n.27+119A=
ENST00000541756.5:c.570A=	ENSP00000446360.2:p.Thr190=
XM_005273978.3:c.834A=	XP_005274035.1:p.Thr278=
XM_005273979.3:c.834A=	XP_005274036.1:p.Thr278=
XM_005273979.4:c.834A=	XP_005274036.1:p.Thr278=
XM_011544999.1:c.768A=	XP_011543301.1:p.Thr256=
XM_011544999.2:c.768A=	XP_011543301.1:p.Thr256=
XM_011545000.1:c.834A=	XP_011543302.1:p.Thr278=
XM_024448501.1:c.834A=	XP_024304269.1:p.Thr278=
XM_024448502.1:c.834A=	XP_024304270.1:p.Thr278=
XM_024448503.1:c.804A=	XP_024304271.1:p.Thr268=
XM_024448504.1:c.768A=	XP_024304272.1:p.Thr256=
XM_024448505.1:c.834A=	XP_024304273.1:p.Thr278=