Canonical Allele Identifier: CA224429427

Gene: INPPL1

Linked Data

• dbSNP Id: rs993984898
• gnomAD v3: 11-72225320-TGAG-T
• gnomAD v4: 11-72225320-TGAG-T
• MyVariant Identifiers: chr11:g.71936365_71936367del (hg19) ; chr11:g.72225321_72225323del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225325_72225327del , CM000673.2:g.72225325_72225327del	GRCh38
NC_000011.9:g.71936369_71936371del , CM000673.1:g.71936369_71936371del	GRCh37
NC_000011.8:g.71614017_71614019del	NCBI36
NG_023253.1:g.5488_5490del
NG_023253.2:g.5488_5490del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+159_182+161del MANE Select	ENSP00000298229.2:n.182+159_182+161del
ENST00000298229.6:c.182+159_182+161del	ENSP00000298229.2:n.182+159_182+161del
ENST00000541544.1:n.98+159_98+161del
NM_001567.3:c.182+159_182+161del	NP_001558.3:n.182+159_182+161del
XM_005273978.3:c.182+159_182+161del	XP_005274035.1:n.182+159_182+161del
XM_005273979.3:c.182+159_182+161del	XP_005274036.1:n.182+159_182+161del
XM_011544999.1:c.182+159_182+161del	XP_011543301.1:n.182+159_182+161del
XM_011545000.1:c.182+159_182+161del	XP_011543302.1:n.182+159_182+161del
XM_005273979.4:c.182+159_182+161del	XP_005274036.1:n.182+159_182+161del
XM_011544999.2:c.182+159_182+161del	XP_011543301.1:n.182+159_182+161del
XM_024448501.1:c.182+159_182+161del	XP_024304269.1:n.182+159_182+161del
XM_024448502.1:c.182+159_182+161del	XP_024304270.1:n.182+159_182+161del
XM_024448503.1:c.62-125_62-123del	XP_024304271.1:n.62-125_62-123del
XM_024448504.1:c.182+159_182+161del	XP_024304272.1:n.182+159_182+161del
XM_024448505.1:c.182+159_182+161del	XP_024304273.1:n.182+159_182+161del
NM_001567.4:c.182+159_182+161del MANE Select	NP_001558.3:n.182+159_182+161del