Canonical Allele Identifier: CA381723426

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71941056C>T (hg19) ; chr11:g.72230012C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230012C>T , CM000673.2:g.72230012C>T	GRCh38
NC_000011.9:g.71941056C>T , CM000673.1:g.71941056C>T	GRCh37
NC_000011.8:g.71618704C>T	NCBI36
NG_023253.1:g.10175C>T
NG_023253.2:g.10175C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.932C>T MANE Select	ENSP00000298229.2:p.Ala311Val
ENST00000298229.6:c.932C>T	ENSP00000298229.2:p.Ala311Val
ENST00000538751.5:c.206C>T	ENSP00000444619.1:p.Ala69Val
ENST00000540329.5:c.116C>T	ENSP00000440018.1:p.Ala39Val
ENST00000541756.5:c.734C>T	ENSP00000446360.2:p.Ala245Val
NM_001567.3:c.932C>T	NP_001558.3:p.Ala311Val
XM_005273978.3:c.998C>T	XP_005274035.1:p.Ala333Val
XM_005273979.3:c.998C>T	XP_005274036.1:p.Ala333Val
XM_011544999.1:c.932C>T	XP_011543301.1:p.Ala311Val
XM_011545000.1:c.998C>T	XP_011543302.1:p.Ala333Val
XM_005273979.4:c.998C>T	XP_005274036.1:p.Ala333Val
XM_011544999.2:c.932C>T	XP_011543301.1:p.Ala311Val
XM_024448501.1:c.998C>T	XP_024304269.1:p.Ala333Val
XM_024448502.1:c.998C>T	XP_024304270.1:p.Ala333Val
XM_024448503.1:c.968C>T	XP_024304271.1:p.Ala323Val
XM_024448504.1:c.932C>T	XP_024304272.1:p.Ala311Val
XM_024448505.1:c.998C>T	XP_024304273.1:p.Ala333Val
NM_001567.4:c.932C>T MANE Select	NP_001558.3:p.Ala311Val