Canonical Allele Identifier: CA2614932163

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72230271-AGTGAGCCAGGGCCAGACCTGGGAGGGGTGGGCAGGGCGGAGCCCCTGGCCTAGGGGCACAGGCCCATGTGACCGGTCCTCCATGCCCTAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230272_72230361del , CM000673.2:g.72230272_72230361del	GRCh38
NC_000011.9:g.71941316_71941405del , CM000673.1:g.71941316_71941405del	GRCh37
NC_000011.8:g.71618964_71619053del	NCBI36
NG_023253.1:g.10435_10524del
NG_023253.2:g.10435_10524del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298229.7:c.1090+1_1091-1del MANE Select	ENSP00000298229.2:n.1090+1_1091-1del
ENST00000298229.6:c.1090+1_1091-1del	ENSP00000298229.2:n.1090+1_1091-1del
ENST00000538751.5:c.364+1_365-1del	ENSP00000444619.1:n.364+1_365-1del
ENST00000540329.5:c.274+1_275-1del	ENSP00000440018.1:n.274+1_275-1del
ENST00000541756.5:c.892+1_893-1del	ENSP00000446360.2:n.892+1_893-1del
NM_001567.3:c.1090+1_1091-1del	NP_001558.3:n.1090+1_1091-1del
XM_005273978.3:c.1156+1_1157-1del	XP_005274035.1:n.1156+1_1157-1del
XM_005273979.3:c.1156+1_1157-1del	XP_005274036.1:n.1156+1_1157-1del
XM_011544999.1:c.1090+1_1091-1del	XP_011543301.1:n.1090+1_1091-1del
XM_011545000.1:c.1156+1_1157-1del	XP_011543302.1:n.1156+1_1157-1del
XM_005273979.4:c.1156+1_1157-1del	XP_005274036.1:n.1156+1_1157-1del
XM_011544999.2:c.1090+1_1091-1del	XP_011543301.1:n.1090+1_1091-1del
XM_024448501.1:c.1156+1_1157-1del	XP_024304269.1:n.1156+1_1157-1del
XM_024448502.1:c.1156+1_1157-1del	XP_024304270.1:n.1156+1_1157-1del
XM_024448503.1:c.1126+1_1127-1del	XP_024304271.1:n.1126+1_1127-1del
XM_024448504.1:c.1090+1_1091-1del	XP_024304272.1:n.1090+1_1091-1del
XM_024448505.1:c.1156+1_1157-1del	XP_024304273.1:n.1156+1_1157-1del
NM_001567.4:c.1090+1_1091-1del MANE Select	NP_001558.3:n.1090+1_1091-1del