Canonical Allele Identifier: CA6169824

Gene: INPPL1

Linked Data

• dbSNP Id: rs371907420
• ExAC: 11:71941000 A / G
• gnomAD v2: 11-71941000-A-G
• gnomAD v3: 11-72229956-A-G
• gnomAD v4: 11-72229956-A-G
• MyVariant Identifiers: chr11:g.71941000A>G (hg19) ; chr11:g.72229956A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229956A>G , CM000673.2:g.72229956A>G	GRCh38
NC_000011.9:g.71941000A>G , CM000673.1:g.71941000A>G	GRCh37
NC_000011.8:g.71618648A>G	NCBI36
NG_023253.1:g.10119A>G
NG_023253.2:g.10119A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.876A>G MANE Select	ENSP00000298229.2:p.Thr292=
ENST00000298229.6:c.876A>G	ENSP00000298229.2:p.Thr292=
ENST00000538751.5:c.150A>G	ENSP00000444619.1:p.Thr50=
ENST00000540329.5:c.60A>G	ENSP00000440018.1:p.Thr20=
ENST00000541756.5:c.678A>G	ENSP00000446360.2:p.Thr226=
NM_001567.3:c.876A>G	NP_001558.3:p.Thr292=
XM_005273978.3:c.942A>G	XP_005274035.1:p.Thr314=
XM_005273979.3:c.942A>G	XP_005274036.1:p.Thr314=
XM_011544999.1:c.876A>G	XP_011543301.1:p.Thr292=
XM_011545000.1:c.942A>G	XP_011543302.1:p.Thr314=
XM_005273979.4:c.942A>G	XP_005274036.1:p.Thr314=
XM_011544999.2:c.876A>G	XP_011543301.1:p.Thr292=
XM_024448501.1:c.942A>G	XP_024304269.1:p.Thr314=
XM_024448502.1:c.942A>G	XP_024304270.1:p.Thr314=
XM_024448503.1:c.912A>G	XP_024304271.1:p.Thr304=
XM_024448504.1:c.876A>G	XP_024304272.1:p.Thr292=
XM_024448505.1:c.942A>G	XP_024304273.1:p.Thr314=
NM_001567.4:c.876A>G MANE Select	NP_001558.3:p.Thr292=