Canonical Allele Identifier: CA6170105
Gene: INPPL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72232311_72232315del , CM000673.2:g.72232311_72232315del GRCh38
NC_000011.9:g.71943355_71943359del , CM000673.1:g.71943355_71943359del GRCh37
NC_000011.8:g.71621003_71621007del NCBI36
NG_023253.1:g.12474_12478del
NG_023253.2:g.12474_12478del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298229.7:c.1687_1691del MANE Select ENSP00000298229.2:p.Thr563GlyfsTer3
ENST00000298229.6:c.1687_1691del ENSP00000298229.2:p.Thr563GlyfsTer3
ENST00000537755.1:n.238_242del
ENST00000538751.5:c.961_965del ENSP00000444619.1:p.Thr321GlyfsTer3
ENST00000541756.5:c.1489_1493del ENSP00000446360.2:p.Thr497GlyfsTer3
ENST00000544806.1:n.438_442del
NM_001567.3:c.1687_1691del NP_001558.3:p.Thr563GlyfsTer3
XM_005273978.3:c.1753_1757del XP_005274035.1:p.Thr585GlyfsTer3
XM_005273979.3:c.1753_1757del XP_005274036.1:p.Thr585GlyfsTer3
XM_011544999.1:c.1687_1691del XP_011543301.1:p.Thr563GlyfsTer3
XM_011545000.1:c.1753_1757del XP_011543302.1:p.Thr585GlyfsTer3
XM_005273979.4:c.1753_1757del XP_005274036.1:p.Thr585GlyfsTer3
XM_011544999.2:c.1687_1691del XP_011543301.1:p.Thr563GlyfsTer3
XM_024448501.1:c.1753_1757del XP_024304269.1:p.Thr585GlyfsTer3
XM_024448502.1:c.1753_1757del XP_024304270.1:p.Thr585GlyfsTer3
XM_024448503.1:c.1723_1727del XP_024304271.1:p.Thr575GlyfsTer3
XM_024448504.1:c.1687_1691del XP_024304272.1:p.Thr563GlyfsTer3
XM_024448505.1:c.1753_1757del XP_024304273.1:p.Thr585GlyfsTer3
NM_001567.4:c.1687_1691del MANE Select NP_001558.3:p.Thr563GlyfsTer3
Search 100 bp 5'
Search 100 bp 3'