Canonical Allele Identifier: CA381725058

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71941408C>A (hg19) ; chr11:g.72230364C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230364C>A , CM000673.2:g.72230364C>A	GRCh38
NC_000011.9:g.71941408C>A , CM000673.1:g.71941408C>A	GRCh37
NC_000011.8:g.71619056C>A	NCBI36
NG_023253.1:g.10527C>A
NG_023253.2:g.10527C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1093C>A MANE Select	ENSP00000298229.2:p.Arg365Ser
ENST00000298229.6:c.1093C>A	ENSP00000298229.2:p.Arg365Ser
ENST00000538751.5:c.367C>A	ENSP00000444619.1:p.Arg123Ser
ENST00000540329.5:c.277C>A	ENSP00000440018.1:p.Arg93Ser
ENST00000541756.5:c.895C>A	ENSP00000446360.2:p.Arg299Ser
NM_001567.3:c.1093C>A	NP_001558.3:p.Arg365Ser
XM_005273978.3:c.1159C>A	XP_005274035.1:p.Arg387Ser
XM_005273979.3:c.1159C>A	XP_005274036.1:p.Arg387Ser
XM_011544999.1:c.1093C>A	XP_011543301.1:p.Arg365Ser
XM_011545000.1:c.1159C>A	XP_011543302.1:p.Arg387Ser
XM_005273979.4:c.1159C>A	XP_005274036.1:p.Arg387Ser
XM_011544999.2:c.1093C>A	XP_011543301.1:p.Arg365Ser
XM_024448501.1:c.1159C>A	XP_024304269.1:p.Arg387Ser
XM_024448502.1:c.1159C>A	XP_024304270.1:p.Arg387Ser
XM_024448503.1:c.1129C>A	XP_024304271.1:p.Arg377Ser
XM_024448504.1:c.1093C>A	XP_024304272.1:p.Arg365Ser
XM_024448505.1:c.1159C>A	XP_024304273.1:p.Arg387Ser
NM_001567.4:c.1093C>A MANE Select	NP_001558.3:p.Arg365Ser