Canonical Allele Identifier: CA679972437

Gene: INPPL1

Linked Data

• dbSNP Id: rs1442865975
• gnomAD v4: 11-72224703-G-A
• MyVariant Identifiers: chr11:g.71935747G>A (hg19) ; chr11:g.72224703G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224703G>A , CM000673.2:g.72224703G>A	GRCh38
NC_000011.9:g.71935747G>A , CM000673.1:g.71935747G>A	GRCh37
NC_000011.8:g.71613395G>A	NCBI36
NG_023253.1:g.4866G>A
NG_023253.2:g.4866G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540973.1:c.-205-77G>A	ENSP00000440904.1:n.-205-77G>A
ENST00000543234.1:c.-205-77G>A	ENSP00000440512.1:n.-205-77G>A
XM_005273978.3:c.-205-77G>A	XP_005274035.1:n.-205-77G>A
XM_005273979.3:c.-205-77G>A	XP_005274036.1:n.-205-77G>A
XM_011544999.1:c.-205-77G>A	XP_011543301.1:n.-205-77G>A
XM_011545000.1:c.-205-77G>A	XP_011543302.1:n.-205-77G>A
XM_005273979.4:c.-205-77G>A	XP_005274036.1:n.-205-77G>A
XM_011544999.2:c.-205-77G>A	XP_011543301.1:n.-205-77G>A
XM_024448501.1:c.-205-77G>A	XP_024304269.1:n.-205-77G>A
XM_024448502.1:c.-205-77G>A	XP_024304270.1:n.-205-77G>A
XM_024448503.1:c.-326-77G>A	XP_024304271.1:n.-326-77G>A
XM_024448504.1:c.-205-77G>A	XP_024304272.1:n.-205-77G>A
XM_024448505.1:c.-205-77G>A	XP_024304273.1:n.-205-77G>A