Canonical Allele Identifier: CA475865971

Gene: INPPL1

Linked Data

• dbSNP Id: rs1317494230
• gnomAD v2: 11-71941192-C-T
• gnomAD v3: 11-72230148-C-T
• gnomAD v4: 11-72230148-C-T
• MyVariant Identifiers: chr11:g.71941192C>T (hg19) ; chr11:g.72230148C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230148C>T , CM000673.2:g.72230148C>T	GRCh38
NC_000011.9:g.71941192C>T , CM000673.1:g.71941192C>T	GRCh37
NC_000011.8:g.71618840C>T	NCBI36
NG_023253.1:g.10311C>T
NG_023253.2:g.10311C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.967C>T MANE Select	ENSP00000298229.2:p.Leu323=
ENST00000298229.6:c.967C>T	ENSP00000298229.2:p.Leu323=
ENST00000538751.5:c.241C>T	ENSP00000444619.1:p.Leu81=
ENST00000540329.5:c.151C>T	ENSP00000440018.1:p.Leu51=
ENST00000541756.5:c.769C>T	ENSP00000446360.2:p.Leu257=
NM_001567.3:c.967C>T	NP_001558.3:p.Leu323=
XM_005273978.3:c.1033C>T	XP_005274035.1:p.Leu345=
XM_005273979.3:c.1033C>T	XP_005274036.1:p.Leu345=
XM_011544999.1:c.967C>T	XP_011543301.1:p.Leu323=
XM_011545000.1:c.1033C>T	XP_011543302.1:p.Leu345=
XM_005273979.4:c.1033C>T	XP_005274036.1:p.Leu345=
XM_011544999.2:c.967C>T	XP_011543301.1:p.Leu323=
XM_024448501.1:c.1033C>T	XP_024304269.1:p.Leu345=
XM_024448502.1:c.1033C>T	XP_024304270.1:p.Leu345=
XM_024448503.1:c.1003C>T	XP_024304271.1:p.Leu335=
XM_024448504.1:c.967C>T	XP_024304272.1:p.Leu323=
XM_024448505.1:c.1033C>T	XP_024304273.1:p.Leu345=
NM_001567.4:c.967C>T MANE Select	NP_001558.3:p.Leu323=