Canonical Allele Identifier: CA2838914938

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230336dup , CM000673.2:g.72230336dup	GRCh38
NC_000011.9:g.71941380dup , CM000673.1:g.71941380dup	GRCh37
NC_000011.8:g.71619028dup	NCBI36
NG_023253.1:g.10499dup
NG_023253.2:g.10499dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1091-26dup MANE Select	ENSP00000298229.2:n.1091-26dup
ENST00000298229.6:c.1091-26dup	ENSP00000298229.2:n.1091-26dup
ENST00000538751.5:c.365-26dup	ENSP00000444619.1:n.365-26dup
ENST00000540329.5:c.275-26dup	ENSP00000440018.1:n.275-26dup
ENST00000541756.5:c.893-26dup	ENSP00000446360.2:n.893-26dup
NM_001567.3:c.1091-26dup	NP_001558.3:n.1091-26dup
XM_005273978.3:c.1157-26dup	XP_005274035.1:n.1157-26dup
XM_005273979.3:c.1157-26dup	XP_005274036.1:n.1157-26dup
XM_011544999.1:c.1091-26dup	XP_011543301.1:n.1091-26dup
XM_011545000.1:c.1157-26dup	XP_011543302.1:n.1157-26dup
XM_005273979.4:c.1157-26dup	XP_005274036.1:n.1157-26dup
XM_011544999.2:c.1091-26dup	XP_011543301.1:n.1091-26dup
XM_024448501.1:c.1157-26dup	XP_024304269.1:n.1157-26dup
XM_024448502.1:c.1157-26dup	XP_024304270.1:n.1157-26dup
XM_024448503.1:c.1127-26dup	XP_024304271.1:n.1127-26dup
XM_024448504.1:c.1091-26dup	XP_024304272.1:n.1091-26dup
XM_024448505.1:c.1157-26dup	XP_024304273.1:n.1157-26dup
NM_001567.4:c.1091-26dup MANE Select	NP_001558.3:n.1091-26dup