Canonical Allele Identifier: CA381755326

Gene: INPPL1

Linked Data

• ClinVar Variation Id: 2318629
• ClinVar RCV Id: RCV002910728
• MyVariant Identifiers: chr11:g.71936129T>G (hg19) ; chr11:g.72225085T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225085T>G , CM000673.2:g.72225085T>G	GRCh38
NC_000011.9:g.71936129T>G , CM000673.1:g.71936129T>G	GRCh37
NC_000011.8:g.71613777T>G	NCBI36
NG_023253.1:g.5248T>G
NG_023253.2:g.5248T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.101T>G MANE Select	ENSP00000298229.2:p.Leu34Arg
ENST00000298229.6:c.101T>G	ENSP00000298229.2:p.Leu34Arg
ENST00000541544.1:n.17T>G
NM_001567.3:c.101T>G	NP_001558.3:p.Leu34Arg
XM_005273978.3:c.101T>G	XP_005274035.1:p.Leu34Arg
XM_005273979.3:c.101T>G	XP_005274036.1:p.Leu34Arg
XM_011544999.1:c.101T>G	XP_011543301.1:p.Leu34Arg
XM_011545000.1:c.101T>G	XP_011543302.1:p.Leu34Arg
XM_005273979.4:c.101T>G	XP_005274036.1:p.Leu34Arg
XM_011544999.2:c.101T>G	XP_011543301.1:p.Leu34Arg
XM_024448501.1:c.101T>G	XP_024304269.1:p.Leu34Arg
XM_024448502.1:c.101T>G	XP_024304270.1:p.Leu34Arg
XM_024448503.1:c.-21T>G	XP_024304271.1:n.-21T>G
XM_024448504.1:c.101T>G	XP_024304272.1:p.Leu34Arg
XM_024448505.1:c.101T>G	XP_024304273.1:p.Leu34Arg
NM_001567.4:c.101T>G MANE Select	NP_001558.3:p.Leu34Arg