Canonical Allele Identifier: CA475606220

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71936067C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225023C>G , CM000673.2:g.72225023C>G	GRCh38
NC_000011.9:g.71936067C>G , CM000673.1:g.71936067C>G	GRCh37
NC_000011.8:g.71613715C>G	NCBI36
NG_023253.1:g.5186C>G
NG_023253.2:g.5186C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.39C>G MANE Select	ENSP00000298229.2:p.Ala13=
ENST00000298229.6:c.39C>G	ENSP00000298229.2:p.Ala13=
ENST00000540973.1:c.39C>G	ENSP00000440904.1:p.Ala13=
ENST00000543234.1:c.39C>G	ENSP00000440512.1:p.Ala13=
NM_001567.3:c.39C>G	NP_001558.3:p.Ala13=
XM_005273978.3:c.39C>G	XP_005274035.1:p.Ala13=
XM_005273979.3:c.39C>G	XP_005274036.1:p.Ala13=
XM_011544999.1:c.39C>G	XP_011543301.1:p.Ala13=
XM_011545000.1:c.39C>G	XP_011543302.1:p.Ala13=
XM_005273979.4:c.39C>G	XP_005274036.1:p.Ala13=
XM_011544999.2:c.39C>G	XP_011543301.1:p.Ala13=
XM_024448501.1:c.39C>G	XP_024304269.1:p.Ala13=
XM_024448502.1:c.39C>G	XP_024304270.1:p.Ala13=
XM_024448503.1:c.-83C>G	XP_024304271.1:n.-83C>G
XM_024448504.1:c.39C>G	XP_024304272.1:p.Ala13=
XM_024448505.1:c.39C>G	XP_024304273.1:p.Ala13=
NM_001567.4:c.39C>G MANE Select	NP_001558.3:p.Ala13=