Canonical Allele Identifier: CA679972467

Gene: INPPL1

Linked Data

• dbSNP Id: rs1439539229
• gnomAD v3: 11-72224778-A-G
• gnomAD v4: 11-72224778-A-G
• MyVariant Identifiers: chr11:g.71935822A>G (hg19) ; chr11:g.72224778A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224778A>G , CM000673.2:g.72224778A>G	GRCh38
NC_000011.9:g.71935822A>G , CM000673.1:g.71935822A>G	GRCh37
NC_000011.8:g.71613470A>G	NCBI36
NG_023253.1:g.4941A>G
NG_023253.2:g.4941A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.-207A>G MANE Select	ENSP00000298229.2:n.-207A>G
ENST00000540973.1:c.-205-2A>G	ENSP00000440904.1:n.-205-2A>G
ENST00000543234.1:c.-205-2A>G	ENSP00000440512.1:n.-205-2A>G
XM_005273978.3:c.-205-2A>G	XP_005274035.1:n.-205-2A>G
XM_005273979.3:c.-205-2A>G	XP_005274036.1:n.-205-2A>G
XM_011544999.1:c.-205-2A>G	XP_011543301.1:n.-205-2A>G
XM_011545000.1:c.-205-2A>G	XP_011543302.1:n.-205-2A>G
XM_005273979.4:c.-205-2A>G	XP_005274036.1:n.-205-2A>G
XM_011544999.2:c.-205-2A>G	XP_011543301.1:n.-205-2A>G
XM_024448501.1:c.-205-2A>G	XP_024304269.1:n.-205-2A>G
XM_024448502.1:c.-205-2A>G	XP_024304270.1:n.-205-2A>G
XM_024448503.1:c.-326-2A>G	XP_024304271.1:n.-326-2A>G
XM_024448504.1:c.-205-2A>G	XP_024304272.1:n.-205-2A>G
XM_024448505.1:c.-205-2A>G	XP_024304273.1:n.-205-2A>G
NM_001567.4:c.-207A>G MANE Select	NP_001558.3:n.-207A>G