Canonical Allele Identifier: CA679973028

Gene: INPPL1

Linked Data

• dbSNP Id: rs1198190944
• gnomAD v3: 11-72225343-C-A
• gnomAD v4: 11-72225343-C-A
• MyVariant Identifiers: chr11:g.71936387C>A (hg19) ; chr11:g.72225343C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225343C>A , CM000673.2:g.72225343C>A	GRCh38
NC_000011.9:g.71936387C>A , CM000673.1:g.71936387C>A	GRCh37
NC_000011.8:g.71614035C>A	NCBI36
NG_023253.1:g.5506C>A
NG_023253.2:g.5506C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+177C>A MANE Select	ENSP00000298229.2:n.182+177C>A
ENST00000298229.6:c.182+177C>A	ENSP00000298229.2:n.182+177C>A
ENST00000541544.1:n.98+177C>A
NM_001567.3:c.182+177C>A	NP_001558.3:n.182+177C>A
XM_005273978.3:c.182+177C>A	XP_005274035.1:n.182+177C>A
XM_005273979.3:c.182+177C>A	XP_005274036.1:n.182+177C>A
XM_011544999.1:c.182+177C>A	XP_011543301.1:n.182+177C>A
XM_011545000.1:c.182+177C>A	XP_011543302.1:n.182+177C>A
XM_005273979.4:c.182+177C>A	XP_005274036.1:n.182+177C>A
XM_011544999.2:c.182+177C>A	XP_011543301.1:n.182+177C>A
XM_024448501.1:c.182+177C>A	XP_024304269.1:n.182+177C>A
XM_024448502.1:c.182+177C>A	XP_024304270.1:n.182+177C>A
XM_024448503.1:c.62-107C>A	XP_024304271.1:n.62-107C>A
XM_024448504.1:c.182+177C>A	XP_024304272.1:n.182+177C>A
XM_024448505.1:c.182+177C>A	XP_024304273.1:n.182+177C>A
NM_001567.4:c.182+177C>A MANE Select	NP_001558.3:n.182+177C>A