Canonical Allele Identifier: CA381725019

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72230360-A-T
• MyVariant Identifiers: chr11:g.71941404A>T (hg19) ; chr11:g.72230360A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230360A>T , CM000673.2:g.72230360A>T	GRCh38
NC_000011.9:g.71941404A>T , CM000673.1:g.71941404A>T	GRCh37
NC_000011.8:g.71619052A>T	NCBI36
NG_023253.1:g.10523A>T
NG_023253.2:g.10523A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1091-2A>T MANE Select	ENSP00000298229.2:n.1091-2A>T
ENST00000298229.6:c.1091-2A>T	ENSP00000298229.2:n.1091-2A>T
ENST00000538751.5:c.365-2A>T	ENSP00000444619.1:n.365-2A>T
ENST00000540329.5:c.275-2A>T	ENSP00000440018.1:n.275-2A>T
ENST00000541756.5:c.893-2A>T	ENSP00000446360.2:n.893-2A>T
NM_001567.3:c.1091-2A>T	NP_001558.3:n.1091-2A>T
XM_005273978.3:c.1157-2A>T	XP_005274035.1:n.1157-2A>T
XM_005273979.3:c.1157-2A>T	XP_005274036.1:n.1157-2A>T
XM_011544999.1:c.1091-2A>T	XP_011543301.1:n.1091-2A>T
XM_011545000.1:c.1157-2A>T	XP_011543302.1:n.1157-2A>T
XM_005273979.4:c.1157-2A>T	XP_005274036.1:n.1157-2A>T
XM_011544999.2:c.1091-2A>T	XP_011543301.1:n.1091-2A>T
XM_024448501.1:c.1157-2A>T	XP_024304269.1:n.1157-2A>T
XM_024448502.1:c.1157-2A>T	XP_024304270.1:n.1157-2A>T
XM_024448503.1:c.1127-2A>T	XP_024304271.1:n.1127-2A>T
XM_024448504.1:c.1091-2A>T	XP_024304272.1:n.1091-2A>T
XM_024448505.1:c.1157-2A>T	XP_024304273.1:n.1157-2A>T
NM_001567.4:c.1091-2A>T MANE Select	NP_001558.3:n.1091-2A>T