Canonical Allele Identifier: CA2614932284

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72230584-G-GACCTACCCCTGCCAGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230584_72230585insACCTACCCCTGCCAGGA , CM000673.2:g.72230584_72230585insACCTACCCCTGCCAGGA	GRCh38
NC_000011.9:g.71941628_71941629insACCTACCCCTGCCAGGA , CM000673.1:g.71941628_71941629insACCTACCCCTGCCAGGA	GRCh37
NC_000011.8:g.71619276_71619277insACCTACCCCTGCCAGGA	NCBI36
NG_023253.1:g.10747_10748insACCTACCCCTGCCAGGA
NG_023253.2:g.10747_10748insACCTACCCCTGCCAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1197+116_1197+117insACCTACCCCTGCCAGGA MANE Select	ENSP00000298229.2:n.1197+116_1197+117insACCTACCCCTGCCAGGA
ENST00000298229.6:c.1197+116_1197+117insACCTACCCCTGCCAGGA	ENSP00000298229.2:n.1197+116_1197+117insACCTACCCCTGCCAGGA
ENST00000538751.5:c.471+116_471+117insACCTACCCCTGCCAGGA	ENSP00000444619.1:n.471+116_471+117insACCTACCCCTGCCAGGA
ENST00000541756.5:c.999+116_999+117insACCTACCCCTGCCAGGA	ENSP00000446360.2:n.999+116_999+117insACCTACCCCTGCCAGGA
NM_001567.3:c.1197+116_1197+117insACCTACCCCTGCCAGGA	NP_001558.3:n.1197+116_1197+117insACCTACCCCTGCCAGGA
XM_005273978.3:c.1263+116_1263+117insACCTACCCCTGCCAGGA	XP_005274035.1:n.1263+116_1263+117insACCTACCCCTGCCAGGA
XM_005273979.3:c.1263+116_1263+117insACCTACCCCTGCCAGGA	XP_005274036.1:n.1263+116_1263+117insACCTACCCCTGCCAGGA
XM_011544999.1:c.1197+116_1197+117insACCTACCCCTGCCAGGA	XP_011543301.1:n.1197+116_1197+117insACCTACCCCTGCCAGGA
XM_011545000.1:c.1263+116_1263+117insACCTACCCCTGCCAGGA	XP_011543302.1:n.1263+116_1263+117insACCTACCCCTGCCAGGA
XM_005273979.4:c.1263+116_1263+117insACCTACCCCTGCCAGGA	XP_005274036.1:n.1263+116_1263+117insACCTACCCCTGCCAGGA
XM_011544999.2:c.1197+116_1197+117insACCTACCCCTGCCAGGA	XP_011543301.1:n.1197+116_1197+117insACCTACCCCTGCCAGGA
XM_024448501.1:c.1263+116_1263+117insACCTACCCCTGCCAGGA	XP_024304269.1:n.1263+116_1263+117insACCTACCCCTGCCAGGA
XM_024448502.1:c.1263+116_1263+117insACCTACCCCTGCCAGGA	XP_024304270.1:n.1263+116_1263+117insACCTACCCCTGCCAGGA
XM_024448503.1:c.1233+116_1233+117insACCTACCCCTGCCAGGA	XP_024304271.1:n.1233+116_1233+117insACCTACCCCTGCCAGGA
XM_024448504.1:c.1197+116_1197+117insACCTACCCCTGCCAGGA	XP_024304272.1:n.1197+116_1197+117insACCTACCCCTGCCAGGA
XM_024448505.1:c.1263+116_1263+117insACCTACCCCTGCCAGGA	XP_024304273.1:n.1263+116_1263+117insACCTACCCCTGCCAGGA
NM_001567.4:c.1197+116_1197+117insACCTACCCCTGCCAGGA MANE Select	NP_001558.3:n.1197+116_1197+117insACCTACCCCTGCCAGGA