Canonical Allele Identifier: CA381733831

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72234279A>C , CM000673.2:g.72234279A>C	GRCh38
NC_000011.9:g.71945323A>C , CM000673.1:g.71945323A>C	GRCh37
NC_000011.8:g.71622971A>C	NCBI36
NG_023253.1:g.14442A>C
NG_023253.2:g.14442A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001567.4:c.2213-2A>C MANE Select	NP_001558.3:n.2213-2A>C
ENST00000298229.7:c.2213-2A>C MANE Select	ENSP00000298229.2:n.2213-2A>C
NM_001567.3:c.2213-2A>C	NP_001558.3:n.2213-2A>C
ENST00000298229.6:c.2213-2A>C	ENSP00000298229.2:n.2213-2A>C
ENST00000535985.1:c.66-2A>C
ENST00000538751.5:c.1487-2A>C	ENSP00000444619.1:n.1487-2A>C
ENST00000541303.5:n.819-2A>C
ENST00000541756.5:c.2015-2A>C	ENSP00000446360.2:n.2015-2A>C
ENST00000545355.5:n.498-2A>C
XM_005273978.3:c.2279-2A>C	XP_005274035.1:n.2279-2A>C
XM_005273979.3:c.2279-2A>C	XP_005274036.1:n.2279-2A>C
XM_005273979.4:c.2279-2A>C	XP_005274036.1:n.2279-2A>C
XM_011544999.1:c.2213-2A>C	XP_011543301.1:n.2213-2A>C
XM_011544999.2:c.2213-2A>C	XP_011543301.1:n.2213-2A>C
XM_011545000.1:c.2279-2A>C	XP_011543302.1:n.2279-2A>C
XM_024448501.1:c.2411-2A>C	XP_024304269.1:n.2411-2A>C
XM_024448502.1:c.2411-2A>C	XP_024304270.1:n.2411-2A>C
XM_024448503.1:c.2381-2A>C	XP_024304271.1:n.2381-2A>C
XM_024448504.1:c.2345-2A>C	XP_024304272.1:n.2345-2A>C
XM_024448505.1:c.2411-2A>C	XP_024304273.1:n.2411-2A>C