Canonical Allele Identifier: CA2614950795

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72225003-GCGCCGGGCCCGGGGGGCGCCCTGGGCAGCCAGGCCCCCTCCTGGTACCACCGCGACCTGAGCCGGGCGGCCGCGGAGGAGCTGCTGGCCCGGGCGGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225007_72225104del , CM000673.2:g.72225007_72225104del	GRCh38
NC_000011.9:g.71936051_71936148del , CM000673.1:g.71936051_71936148del	GRCh37
NC_000011.8:g.71613699_71613796del	NCBI36
NG_023253.1:g.5170_5267del
NG_023253.2:g.5170_5267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.23_120del MANE Select	ENSP00000298229.2:p.Pro8ArgfsTer?
ENST00000298229.6:c.23_120del	ENSP00000298229.2:p.Pro8ArgfsTer?
NM_001567.3:c.23_120del	NP_001558.3:p.Pro8ArgfsTer?
XM_005273978.3:c.23_120del	XP_005274035.1:p.Pro8ArgfsTer?
XM_005273979.3:c.23_120del	XP_005274036.1:p.Pro8ArgfsTer?
XM_011544999.1:c.23_120del	XP_011543301.1:p.Pro8ArgfsTer?
XM_011545000.1:c.23_120del	XP_011543302.1:p.Pro8ArgfsTer?
XM_005273979.4:c.23_120del	XP_005274036.1:p.Pro8ArgfsTer?
XM_011544999.2:c.23_120del	XP_011543301.1:p.Pro8ArgfsTer?
XM_024448501.1:c.23_120del	XP_024304269.1:p.Pro8ArgfsTer?
XM_024448502.1:c.23_120del	XP_024304270.1:p.Pro8ArgfsTer?
XM_024448503.1:c.-99_-2del	XP_024304271.1:n.-99_-2del
XM_024448504.1:c.23_120del	XP_024304272.1:p.Pro8ArgfsTer?
XM_024448505.1:c.23_120del	XP_024304273.1:p.Pro8ArgfsTer?
NM_001567.4:c.23_120del MANE Select	NP_001558.3:p.Pro8ArgfsTer?