Canonical Allele Identifier: CA2614950730

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72224941-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224941G>A , CM000673.2:g.72224941G>A	GRCh38
NC_000011.9:g.71935985G>A , CM000673.1:g.71935985G>A	GRCh37
NC_000011.8:g.71613633G>A	NCBI36
NG_023253.1:g.5104G>A
NG_023253.2:g.5104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.-44G>A MANE Select	ENSP00000298229.2:n.-44G>A
ENST00000298229.6:c.-44G>A	ENSP00000298229.2:n.-44G>A
ENST00000540973.1:c.-44G>A	ENSP00000440904.1:n.-44G>A
ENST00000543234.1:c.-44G>A	ENSP00000440512.1:n.-44G>A
NM_001567.3:c.-44G>A	NP_001558.3:n.-44G>A
XM_005273978.3:c.-44G>A	XP_005274035.1:n.-44G>A
XM_005273979.3:c.-44G>A	XP_005274036.1:n.-44G>A
XM_011544999.1:c.-44G>A	XP_011543301.1:n.-44G>A
XM_011545000.1:c.-44G>A	XP_011543302.1:n.-44G>A
XM_005273979.4:c.-44G>A	XP_005274036.1:n.-44G>A
XM_011544999.2:c.-44G>A	XP_011543301.1:n.-44G>A
XM_024448501.1:c.-44G>A	XP_024304269.1:n.-44G>A
XM_024448502.1:c.-44G>A	XP_024304270.1:n.-44G>A
XM_024448503.1:c.-165G>A	XP_024304271.1:n.-165G>A
XM_024448504.1:c.-44G>A	XP_024304272.1:n.-44G>A
XM_024448505.1:c.-44G>A	XP_024304273.1:n.-44G>A
NM_001567.4:c.-44G>A MANE Select	NP_001558.3:n.-44G>A