Canonical Allele Identifier: CA2614932014

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72230017-GAGGTACATGGCAGTGGGGCCTCACAGGGCCAAGGGTGGTTGGAGGTGACCAGGGTGCTGCCTACTCCAAGGTCTTGTCAGCAGCCTCCCCACCTGGCCTAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230022_72230122del , CM000673.2:g.72230022_72230122del	GRCh38
NC_000011.9:g.71941066_71941166del , CM000673.1:g.71941066_71941166del	GRCh37
NC_000011.8:g.71618714_71618814del	NCBI36
NG_023253.1:g.10185_10285del
NG_023253.2:g.10185_10285del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.939+3_941del
ENST00000298229.6:c.939+3_941del
ENST00000538751.5:c.213+3_215del
ENST00000540329.5:c.123+3_125del
ENST00000541756.5:c.741+3_743del
NM_001567.3:c.939+3_941del
XM_005273978.3:c.1005+3_1007del
XM_005273979.3:c.1005+3_1007del
XM_011544999.1:c.939+3_941del
XM_011545000.1:c.1005+3_1007del
XM_005273979.4:c.1005+3_1007del
XM_011544999.2:c.939+3_941del
XM_024448501.1:c.1005+3_1007del
XM_024448502.1:c.1005+3_1007del
XM_024448503.1:c.975+3_977del
XM_024448504.1:c.939+3_941del
XM_024448505.1:c.1005+3_1007del
NM_001567.4:c.939+3_941del