Canonical Allele Identifier: CA645372902

Gene: INPPL1

Linked Data

• PubMed: PMID:23273567

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.[72225019dup;72232311_72232315del] , CM000673.2:g.[72225019dup;72232311_72232315del]	GRCh38
NC_000011.9:g.[71936063dup;71943355_71943359del] , CM000673.1:g.[71936063dup;71943355_71943359del]	GRCh37
NC_000011.8:g.[71613711dup;71621003_71621007del]	NCBI36
NG_023253.1:g.[5182dup;12474_12478del]
NG_023253.2:g.[5182dup;12474_12478del]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.[35dup;1687_1691del] MANE Select	ENSP00000298229.2:p.Gly13ArgfsTer62
ENST00000298229.6:c.[35dup;1687_1691del]	ENSP00000298229.2:p.Gly13ArgfsTer62
NM_001567.3:c.[35dup;1687_1691del]	NP_001558.3:p.Gly13ArgfsTer62
XM_005273978.3:c.[35dup;1753_1757del]	XP_005274035.1:p.Gly13ArgfsTer62
XM_005273979.3:c.[35dup;1753_1757del]	XP_005274036.1:p.Gly13ArgfsTer62
XM_011544999.1:c.[35dup;1687_1691del]	XP_011543301.1:p.Gly13ArgfsTer62
XM_011545000.1:c.[35dup;1753_1757del]	XP_011543302.1:p.Gly13ArgfsTer62
XM_005273979.4:c.[35dup;1753_1757del]	XP_005274036.1:p.Gly13ArgfsTer62
XM_011544999.2:c.[35dup;1687_1691del]	XP_011543301.1:p.Gly13ArgfsTer62
XM_024448501.1:c.[35dup;1753_1757del]	XP_024304269.1:p.Gly13ArgfsTer62
XM_024448502.1:c.[35dup;1753_1757del]	XP_024304270.1:p.Gly13ArgfsTer62
XM_024448503.1:c.[-87dup;1723_1727del]	XP_024304271.1:p.Thr575GlyfsTer3
XM_024448504.1:c.[35dup;1687_1691del]	XP_024304272.1:p.Gly13ArgfsTer62
XM_024448505.1:c.[35dup;1753_1757del]	XP_024304273.1:p.Gly13ArgfsTer62
NM_001567.4:c.[35dup;1687_1691del] MANE Select	NP_001558.3:p.Gly13ArgfsTer62