Canonical Allele Identifier: CA1981897872
Gene: INPPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72230005G= , CM000673.2:g.72230005G= GRCh38
NC_000011.9:g.71941049G= , CM000673.1:g.71941049G= GRCh37
NC_000011.8:g.71618697G= NCBI36
NG_023253.1:g.10168G=
NG_023253.2:g.10168G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298229.7:c.925G= MANE Select ENSP00000298229.2:p.Val309=
ENST00000298229.6:c.925G= ENSP00000298229.2:p.Val309=
ENST00000538751.5:c.199G= ENSP00000444619.1:p.Val67=
ENST00000540329.5:c.109G= ENSP00000440018.1:p.Val37=
ENST00000541756.5:c.727G= ENSP00000446360.2:p.Val243=
NM_001567.3:c.925G= NP_001558.3:p.Val309=
XM_005273978.3:c.991G= XP_005274035.1:p.Val331=
XM_005273979.3:c.991G= XP_005274036.1:p.Val331=
XM_011544999.1:c.925G= XP_011543301.1:p.Val309=
XM_011545000.1:c.991G= XP_011543302.1:p.Val331=
XM_005273979.4:c.991G= XP_005274036.1:p.Val331=
XM_011544999.2:c.925G= XP_011543301.1:p.Val309=
XM_024448501.1:c.991G= XP_024304269.1:p.Val331=
XM_024448502.1:c.991G= XP_024304270.1:p.Val331=
XM_024448503.1:c.961G= XP_024304271.1:p.Val321=
XM_024448504.1:c.925G= XP_024304272.1:p.Val309=
XM_024448505.1:c.991G= XP_024304273.1:p.Val331=
NM_001567.4:c.925G= MANE Select NP_001558.3:p.Val309=