Canonical Allele Identifier: CA1981895222

Gene: INPPL1

Linked Data

• dbSNP Id: rs934747323

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224729G>C , CM000673.2:g.72224729G>C	GRCh38
NC_000011.9:g.71935773G>C , CM000673.1:g.71935773G>C	GRCh37
NC_000011.8:g.71613421G>C	NCBI36
NG_023253.1:g.4892G>C
NG_023253.2:g.4892G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540973.1:c.-205-51G>C	ENSP00000440904.1:n.-205-51G>C
ENST00000543234.1:c.-205-51G>C	ENSP00000440512.1:n.-205-51G>C
XM_005273978.3:c.-205-51G>C	XP_005274035.1:n.-205-51G>C
XM_005273979.3:c.-205-51G>C	XP_005274036.1:n.-205-51G>C
XM_011544999.1:c.-205-51G>C	XP_011543301.1:n.-205-51G>C
XM_011545000.1:c.-205-51G>C	XP_011543302.1:n.-205-51G>C
XM_005273979.4:c.-205-51G>C	XP_005274036.1:n.-205-51G>C
XM_011544999.2:c.-205-51G>C	XP_011543301.1:n.-205-51G>C
XM_024448501.1:c.-205-51G>C	XP_024304269.1:n.-205-51G>C
XM_024448502.1:c.-205-51G>C	XP_024304270.1:n.-205-51G>C
XM_024448503.1:c.-326-51G>C	XP_024304271.1:n.-326-51G>C
XM_024448504.1:c.-205-51G>C	XP_024304272.1:n.-205-51G>C
XM_024448505.1:c.-205-51G>C	XP_024304273.1:n.-205-51G>C