Canonical Allele Identifier: CA645372518

Gene: INPPL1

Linked Data

• PubMed: PMID:23273567

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.[72225008_72225023del;72229558G>C] , CM000673.2:g.[72225008_72225023del;72229558G>C]	GRCh38
NC_000011.9:g.[71936052_71936067del;71940602G>C] , CM000673.1:g.[71936052_71936067del;71940602G>C]	GRCh37
NC_000011.8:g.[71613700_71613715del;71618250G>C]	NCBI36
NG_023253.1:g.[5171_5186del;9721G>C]
NG_023253.2:g.[5171_5186del;9721G>C]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.[24_39del;753G>C] MANE Select	ENSP00000298229.2:p.Gly9TrpfsTer13
ENST00000298229.6:c.[24_39del;753G>C]	ENSP00000298229.2:p.Gly9TrpfsTer13
NM_001567.3:c.[24_39del;753G>C]	NP_001558.3:p.Gly9TrpfsTer13
XM_005273978.3:c.[24_39del;819G>C]	XP_005274035.1:p.Gly9TrpfsTer13
XM_005273979.3:c.[24_39del;819G>C]	XP_005274036.1:p.Gly9TrpfsTer13
XM_011544999.1:c.[24_39del;753G>C]	XP_011543301.1:p.Gly9TrpfsTer13
XM_011545000.1:c.[24_39del;819G>C]	XP_011543302.1:p.Gly9TrpfsTer13
XM_005273979.4:c.[24_39del;819G>C]	XP_005274036.1:p.Gly9TrpfsTer13
XM_011544999.2:c.[24_39del;753G>C]	XP_011543301.1:p.Gly9TrpfsTer13
XM_024448501.1:c.[24_39del;819G>C]	XP_024304269.1:p.Gly9TrpfsTer13
XM_024448502.1:c.[24_39del;819G>C]	XP_024304270.1:p.Gly9TrpfsTer13
XM_024448503.1:c.[-98_-83del;789G>C]	XP_024304271.1:p.Gln263His
XM_024448504.1:c.[24_39del;753G>C]	XP_024304272.1:p.Gly9TrpfsTer13
XM_024448505.1:c.[24_39del;819G>C]	XP_024304273.1:p.Gly9TrpfsTer13
NM_001567.4:c.[24_39del;753G>C] MANE Select	NP_001558.3:p.Gly9TrpfsTer13