Canonical Allele Identifier: CA6169853

Gene: INPPL1

Linked Data

• dbSNP Id: rs755708388
• ExAC: 11:71941164 G / C
• gnomAD v2: 11-71941164-G-C
• MyVariant Identifiers: chr11:g.71941164G>C (hg19) ; chr11:g.72230120G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230120G>C , CM000673.2:g.72230120G>C	GRCh38
NC_000011.9:g.71941164G>C , CM000673.1:g.71941164G>C	GRCh37
NC_000011.8:g.71618812G>C	NCBI36
NG_023253.1:g.10283G>C
NG_023253.2:g.10283G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.940-1G>C MANE Select	ENSP00000298229.2:n.940-1G>C
ENST00000298229.6:c.940-1G>C	ENSP00000298229.2:n.940-1G>C
ENST00000538751.5:c.214-1G>C	ENSP00000444619.1:n.214-1G>C
ENST00000540329.5:c.124-1G>C	ENSP00000440018.1:n.124-1G>C
ENST00000541756.5:c.742-1G>C	ENSP00000446360.2:n.742-1G>C
NM_001567.3:c.940-1G>C	NP_001558.3:n.940-1G>C
XM_005273978.3:c.1006-1G>C	XP_005274035.1:n.1006-1G>C
XM_005273979.3:c.1006-1G>C	XP_005274036.1:n.1006-1G>C
XM_011544999.1:c.940-1G>C	XP_011543301.1:n.940-1G>C
XM_011545000.1:c.1006-1G>C	XP_011543302.1:n.1006-1G>C
XM_005273979.4:c.1006-1G>C	XP_005274036.1:n.1006-1G>C
XM_011544999.2:c.940-1G>C	XP_011543301.1:n.940-1G>C
XM_024448501.1:c.1006-1G>C	XP_024304269.1:n.1006-1G>C
XM_024448502.1:c.1006-1G>C	XP_024304270.1:n.1006-1G>C
XM_024448503.1:c.976-1G>C	XP_024304271.1:n.976-1G>C
XM_024448504.1:c.940-1G>C	XP_024304272.1:n.940-1G>C
XM_024448505.1:c.1006-1G>C	XP_024304273.1:n.1006-1G>C
NM_001567.4:c.940-1G>C MANE Select	NP_001558.3:n.940-1G>C