Canonical Allele Identifier: CA381723089

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71941019C>A (hg19) ; chr11:g.72229975C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229975C>A , CM000673.2:g.72229975C>A	GRCh38
NC_000011.9:g.71941019C>A , CM000673.1:g.71941019C>A	GRCh37
NC_000011.8:g.71618667C>A	NCBI36
NG_023253.1:g.10138C>A
NG_023253.2:g.10138C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.895C>A MANE Select	ENSP00000298229.2:p.Pro299Thr
ENST00000298229.6:c.895C>A	ENSP00000298229.2:p.Pro299Thr
ENST00000538751.5:c.169C>A	ENSP00000444619.1:p.Pro57Thr
ENST00000540329.5:c.79C>A	ENSP00000440018.1:p.Pro27Thr
ENST00000541756.5:c.697C>A	ENSP00000446360.2:p.Pro233Thr
NM_001567.3:c.895C>A	NP_001558.3:p.Pro299Thr
XM_005273978.3:c.961C>A	XP_005274035.1:p.Pro321Thr
XM_005273979.3:c.961C>A	XP_005274036.1:p.Pro321Thr
XM_011544999.1:c.895C>A	XP_011543301.1:p.Pro299Thr
XM_011545000.1:c.961C>A	XP_011543302.1:p.Pro321Thr
XM_005273979.4:c.961C>A	XP_005274036.1:p.Pro321Thr
XM_011544999.2:c.895C>A	XP_011543301.1:p.Pro299Thr
XM_024448501.1:c.961C>A	XP_024304269.1:p.Pro321Thr
XM_024448502.1:c.961C>A	XP_024304270.1:p.Pro321Thr
XM_024448503.1:c.931C>A	XP_024304271.1:p.Pro311Thr
XM_024448504.1:c.895C>A	XP_024304272.1:p.Pro299Thr
XM_024448505.1:c.961C>A	XP_024304273.1:p.Pro321Thr
NM_001567.4:c.895C>A MANE Select	NP_001558.3:p.Pro299Thr