Canonical Allele Identifier: CA381736990

Gene: INPPL1

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72237123G>T , CM000673.2:g.72237123G>T	GRCh38
NC_000011.9:g.71948167G>T , CM000673.1:g.71948167G>T	GRCh37
NC_000011.8:g.71625815G>T	NCBI36
NG_008169.1:g.12054C>A
NG_023253.1:g.17286G>T
NG_023253.2:g.17286G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.2880-1G>T MANE Select	ENSP00000298229.2:n.2880-1G>T
ENST00000298229.6:c.2880-1G>T	ENSP00000298229.2:n.2880-1G>T
ENST00000535985.1:c.269-1898G>T
ENST00000538751.5:c.2154-1G>T	ENSP00000444619.1:n.2154-1G>T
ENST00000541756.5:c.2682-1G>T	ENSP00000446360.2:n.2682-1G>T
NM_001567.3:c.2880-1G>T	NP_001558.3:n.2880-1G>T
XM_005273978.3:c.2946-1G>T	XP_005274035.1:n.2946-1G>T
XM_005273979.3:c.2946-1G>T	XP_005274036.1:n.2946-1G>T
XM_011544999.1:c.2880-1G>T	XP_011543301.1:n.2880-1G>T
XM_011545000.1:c.2946-1G>T	XP_011543302.1:n.2946-1G>T
XM_005273979.4:c.2946-1G>T	XP_005274036.1:n.2946-1G>T
XM_011544999.2:c.2880-1G>T	XP_011543301.1:n.2880-1G>T
XM_024448501.1:c.3078-1G>T	XP_024304269.1:n.3078-1G>T
XM_024448502.1:c.3078-1G>T	XP_024304270.1:n.3078-1G>T
XM_024448503.1:c.3048-1G>T	XP_024304271.1:n.3048-1G>T
XM_024448504.1:c.3012-1G>T	XP_024304272.1:n.3012-1G>T
XM_024448505.1:c.3078-1G>T	XP_024304273.1:n.3078-1G>T
NM_001567.4:c.2880-1G>T MANE Select	NP_001558.3:n.2880-1G>T