Canonical Allele Identifier: CA2614950848

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72225180-GGGCTCCTTGCGGGCTGGCGTGGACCGGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225182_72225210del , CM000673.2:g.72225182_72225210del	GRCh38
NC_000011.9:g.71936226_71936254del , CM000673.1:g.71936226_71936254del	GRCh37
NC_000011.8:g.71613874_71613902del	NCBI36
NG_023253.1:g.5345_5373del
NG_023253.2:g.5345_5373del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+16_182+44del MANE Select	ENSP00000298229.2:n.182+16_182+44del
ENST00000298229.6:c.182+16_182+44del	ENSP00000298229.2:n.182+16_182+44del
ENST00000541544.1:n.98+16_98+44del
NM_001567.3:c.182+16_182+44del	NP_001558.3:n.182+16_182+44del
XM_005273978.3:c.182+16_182+44del	XP_005274035.1:n.182+16_182+44del
XM_005273979.3:c.182+16_182+44del	XP_005274036.1:n.182+16_182+44del
XM_011544999.1:c.182+16_182+44del	XP_011543301.1:n.182+16_182+44del
XM_011545000.1:c.182+16_182+44del	XP_011543302.1:n.182+16_182+44del
XM_005273979.4:c.182+16_182+44del	XP_005274036.1:n.182+16_182+44del
XM_011544999.2:c.182+16_182+44del	XP_011543301.1:n.182+16_182+44del
XM_024448501.1:c.182+16_182+44del	XP_024304269.1:n.182+16_182+44del
XM_024448502.1:c.182+16_182+44del	XP_024304270.1:n.182+16_182+44del
XM_024448503.1:c.61+16_61+44del	XP_024304271.1:n.61+16_61+44del
XM_024448504.1:c.182+16_182+44del	XP_024304272.1:n.182+16_182+44del
XM_024448505.1:c.182+16_182+44del	XP_024304273.1:n.182+16_182+44del
NM_001567.4:c.182+16_182+44del MANE Select	NP_001558.3:n.182+16_182+44del