Canonical Allele Identifier: CA6169944

Gene: INPPL1

Linked Data

• dbSNP Id: rs762874618
• ExAC: 11:71941563 TGGGTGCTTCCCATTGGA / T
• gnomAD v2: 11-71941563-TGGGTGCTTCCCATTGGA-T
• gnomAD v3: 11-72230519-TGGGTGCTTCCCATTGGA-T
• gnomAD v4: 11-72230519-TGGGTGCTTCCCATTGGA-T
• MyVariant Identifiers: chr11:g.71941564_71941580del (hg19) ; chr11:g.72230520_72230536del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230524_72230540del , CM000673.2:g.72230524_72230540del	GRCh38
NC_000011.9:g.71941568_71941584del , CM000673.1:g.71941568_71941584del	GRCh37
NC_000011.8:g.71619216_71619232del	NCBI36
NG_023253.1:g.10687_10703del
NG_023253.2:g.10687_10703del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1197+56_1197+72del MANE Select	ENSP00000298229.2:n.1197+56_1197+72del
ENST00000298229.6:c.1197+56_1197+72del	ENSP00000298229.2:n.1197+56_1197+72del
ENST00000538751.5:c.471+56_471+72del	ENSP00000444619.1:n.471+56_471+72del
ENST00000541756.5:c.999+56_999+72del	ENSP00000446360.2:n.999+56_999+72del
NM_001567.3:c.1197+56_1197+72del	NP_001558.3:n.1197+56_1197+72del
XM_005273978.3:c.1263+56_1263+72del	XP_005274035.1:n.1263+56_1263+72del
XM_005273979.3:c.1263+56_1263+72del	XP_005274036.1:n.1263+56_1263+72del
XM_011544999.1:c.1197+56_1197+72del	XP_011543301.1:n.1197+56_1197+72del
XM_011545000.1:c.1263+56_1263+72del	XP_011543302.1:n.1263+56_1263+72del
XM_005273979.4:c.1263+56_1263+72del	XP_005274036.1:n.1263+56_1263+72del
XM_011544999.2:c.1197+56_1197+72del	XP_011543301.1:n.1197+56_1197+72del
XM_024448501.1:c.1263+56_1263+72del	XP_024304269.1:n.1263+56_1263+72del
XM_024448502.1:c.1263+56_1263+72del	XP_024304270.1:n.1263+56_1263+72del
XM_024448503.1:c.1233+56_1233+72del	XP_024304271.1:n.1233+56_1233+72del
XM_024448504.1:c.1197+56_1197+72del	XP_024304272.1:n.1197+56_1197+72del
XM_024448505.1:c.1263+56_1263+72del	XP_024304273.1:n.1263+56_1263+72del
NM_001567.4:c.1197+56_1197+72del MANE Select	NP_001558.3:n.1197+56_1197+72del