Canonical Allele Identifier: CA2614932215

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72230493-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230493A>G , CM000673.2:g.72230493A>G	GRCh38
NC_000011.9:g.71941537A>G , CM000673.1:g.71941537A>G	GRCh37
NC_000011.8:g.71619185A>G	NCBI36
NG_023253.1:g.10656A>G
NG_023253.2:g.10656A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1197+25A>G MANE Select	ENSP00000298229.2:n.1197+25A>G
ENST00000298229.6:c.1197+25A>G	ENSP00000298229.2:n.1197+25A>G
ENST00000538751.5:c.471+25A>G	ENSP00000444619.1:n.471+25A>G
ENST00000541756.5:c.999+25A>G	ENSP00000446360.2:n.999+25A>G
NM_001567.3:c.1197+25A>G	NP_001558.3:n.1197+25A>G
XM_005273978.3:c.1263+25A>G	XP_005274035.1:n.1263+25A>G
XM_005273979.3:c.1263+25A>G	XP_005274036.1:n.1263+25A>G
XM_011544999.1:c.1197+25A>G	XP_011543301.1:n.1197+25A>G
XM_011545000.1:c.1263+25A>G	XP_011543302.1:n.1263+25A>G
XM_005273979.4:c.1263+25A>G	XP_005274036.1:n.1263+25A>G
XM_011544999.2:c.1197+25A>G	XP_011543301.1:n.1197+25A>G
XM_024448501.1:c.1263+25A>G	XP_024304269.1:n.1263+25A>G
XM_024448502.1:c.1263+25A>G	XP_024304270.1:n.1263+25A>G
XM_024448503.1:c.1233+25A>G	XP_024304271.1:n.1233+25A>G
XM_024448504.1:c.1197+25A>G	XP_024304272.1:n.1197+25A>G
XM_024448505.1:c.1263+25A>G	XP_024304273.1:n.1263+25A>G
NM_001567.4:c.1197+25A>G MANE Select	NP_001558.3:n.1197+25A>G