Canonical Allele Identifier: CA2614950849

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72225181-GGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225182_72225183del , CM000673.2:g.72225182_72225183del	GRCh38
NC_000011.9:g.71936226_71936227del , CM000673.1:g.71936226_71936227del	GRCh37
NC_000011.8:g.71613874_71613875del	NCBI36
NG_023253.1:g.5345_5346del
NG_023253.2:g.5345_5346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+16_182+17del MANE Select	ENSP00000298229.2:n.182+16_182+17del
ENST00000298229.6:c.182+16_182+17del	ENSP00000298229.2:n.182+16_182+17del
ENST00000541544.1:n.98+16_98+17del
NM_001567.3:c.182+16_182+17del	NP_001558.3:n.182+16_182+17del
XM_005273978.3:c.182+16_182+17del	XP_005274035.1:n.182+16_182+17del
XM_005273979.3:c.182+16_182+17del	XP_005274036.1:n.182+16_182+17del
XM_011544999.1:c.182+16_182+17del	XP_011543301.1:n.182+16_182+17del
XM_011545000.1:c.182+16_182+17del	XP_011543302.1:n.182+16_182+17del
XM_005273979.4:c.182+16_182+17del	XP_005274036.1:n.182+16_182+17del
XM_011544999.2:c.182+16_182+17del	XP_011543301.1:n.182+16_182+17del
XM_024448501.1:c.182+16_182+17del	XP_024304269.1:n.182+16_182+17del
XM_024448502.1:c.182+16_182+17del	XP_024304270.1:n.182+16_182+17del
XM_024448503.1:c.61+16_61+17del	XP_024304271.1:n.61+16_61+17del
XM_024448504.1:c.182+16_182+17del	XP_024304272.1:n.182+16_182+17del
XM_024448505.1:c.182+16_182+17del	XP_024304273.1:n.182+16_182+17del
NM_001567.4:c.182+16_182+17del MANE Select	NP_001558.3:n.182+16_182+17del