Canonical Allele Identifier: CA2614950820

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72225165-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225168_72225169del , CM000673.2:g.72225168_72225169del	GRCh38
NC_000011.9:g.71936212_71936213del , CM000673.1:g.71936212_71936213del	GRCh37
NC_000011.8:g.71613860_71613861del	NCBI36
NG_023253.1:g.5331_5332del
NG_023253.2:g.5331_5332del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+2_182+3del
ENST00000298229.6:c.182+2_182+3del
ENST00000541544.1:n.98+2_98+3del
NM_001567.3:c.182+2_182+3del
XM_005273978.3:c.182+2_182+3del
XM_005273979.3:c.182+2_182+3del
XM_011544999.1:c.182+2_182+3del
XM_011545000.1:c.182+2_182+3del
XM_005273979.4:c.182+2_182+3del
XM_011544999.2:c.182+2_182+3del
XM_024448501.1:c.182+2_182+3del
XM_024448502.1:c.182+2_182+3del
XM_024448503.1:c.61+2_61+3del
XM_024448504.1:c.182+2_182+3del
XM_024448505.1:c.182+2_182+3del
NM_001567.4:c.182+2_182+3del