Canonical Allele Identifier: CA1981897863
Gene: INPPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72229989G= , CM000673.2:g.72229989G= GRCh38
NC_000011.9:g.71941033G= , CM000673.1:g.71941033G= GRCh37
NC_000011.8:g.71618681G= NCBI36
NG_023253.1:g.10152G=
NG_023253.2:g.10152G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298229.7:c.909G= MANE Select ENSP00000298229.2:p.Lys303=
ENST00000298229.6:c.909G= ENSP00000298229.2:p.Lys303=
ENST00000538751.5:c.183G= ENSP00000444619.1:p.Lys61=
ENST00000540329.5:c.93G= ENSP00000440018.1:p.Lys31=
ENST00000541756.5:c.711G= ENSP00000446360.2:p.Lys237=
NM_001567.3:c.909G= NP_001558.3:p.Lys303=
XM_005273978.3:c.975G= XP_005274035.1:p.Lys325=
XM_005273979.3:c.975G= XP_005274036.1:p.Lys325=
XM_011544999.1:c.909G= XP_011543301.1:p.Lys303=
XM_011545000.1:c.975G= XP_011543302.1:p.Lys325=
XM_005273979.4:c.975G= XP_005274036.1:p.Lys325=
XM_011544999.2:c.909G= XP_011543301.1:p.Lys303=
XM_024448501.1:c.975G= XP_024304269.1:p.Lys325=
XM_024448502.1:c.975G= XP_024304270.1:p.Lys325=
XM_024448503.1:c.945G= XP_024304271.1:p.Lys315=
XM_024448504.1:c.909G= XP_024304272.1:p.Lys303=
XM_024448505.1:c.975G= XP_024304273.1:p.Lys325=
NM_001567.4:c.909G= MANE Select NP_001558.3:p.Lys303=