Canonical Allele Identifier: CA10581437

Gene: INPPL1

Linked Data

• ClinVar Variation Id: 242401
• ClinVar RCV Id: RCV001824132
• dbSNP Id: rs878853119
• MyVariant Identifiers: chr11:g.71936052_71936067del (hg19) ; chr11:g.72225008_72225023del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225008_72225023del , CM000673.2:g.72225008_72225023del	GRCh38
NC_000011.9:g.71936052_71936067del , CM000673.1:g.71936052_71936067del	GRCh37
NC_000011.8:g.71613700_71613715del	NCBI36
NG_023253.1:g.5171_5186del
NG_023253.2:g.5171_5186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.24_39del MANE Select	ENSP00000298229.2:p.Gly9TrpfsTer13
ENST00000298229.6:c.24_39del	ENSP00000298229.2:p.Gly9TrpfsTer13
ENST00000540973.1:c.24_39del	ENSP00000440904.1:p.Gly9TrpfsTer?
ENST00000543234.1:c.24_39del	ENSP00000440512.1:p.Gly9TrpfsTer?
NM_001567.3:c.24_39del	NP_001558.3:p.Gly9TrpfsTer13
XM_005273978.3:c.24_39del	XP_005274035.1:p.Gly9TrpfsTer13
XM_005273979.3:c.24_39del	XP_005274036.1:p.Gly9TrpfsTer13
XM_011544999.1:c.24_39del	XP_011543301.1:p.Gly9TrpfsTer13
XM_011545000.1:c.24_39del	XP_011543302.1:p.Gly9TrpfsTer13
XM_005273979.4:c.24_39del	XP_005274036.1:p.Gly9TrpfsTer13
XM_011544999.2:c.24_39del	XP_011543301.1:p.Gly9TrpfsTer13
XM_024448501.1:c.24_39del	XP_024304269.1:p.Gly9TrpfsTer13
XM_024448502.1:c.24_39del	XP_024304270.1:p.Gly9TrpfsTer13
XM_024448503.1:c.-98_-83del	XP_024304271.1:n.-98_-83del
XM_024448504.1:c.24_39del	XP_024304272.1:p.Gly9TrpfsTer13
XM_024448505.1:c.24_39del	XP_024304273.1:p.Gly9TrpfsTer13
NM_001567.4:c.24_39del MANE Select	NP_001558.3:p.Gly9TrpfsTer13