Canonical Allele Identifier: CA2614950792

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72224983-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224983C>T , CM000673.2:g.72224983C>T	GRCh38
NC_000011.9:g.71936027C>T , CM000673.1:g.71936027C>T	GRCh37
NC_000011.8:g.71613675C>T	NCBI36
NG_023253.1:g.5146C>T
NG_023253.2:g.5146C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.-2C>T MANE Select	ENSP00000298229.2:n.-2C>T
ENST00000298229.6:c.-2C>T	ENSP00000298229.2:n.-2C>T
ENST00000540973.1:c.-2C>T	ENSP00000440904.1:n.-2C>T
ENST00000543234.1:c.-2C>T	ENSP00000440512.1:n.-2C>T
NM_001567.3:c.-2C>T	NP_001558.3:n.-2C>T
XM_005273978.3:c.-2C>T	XP_005274035.1:n.-2C>T
XM_005273979.3:c.-2C>T	XP_005274036.1:n.-2C>T
XM_011544999.1:c.-2C>T	XP_011543301.1:n.-2C>T
XM_011545000.1:c.-2C>T	XP_011543302.1:n.-2C>T
XM_005273979.4:c.-2C>T	XP_005274036.1:n.-2C>T
XM_011544999.2:c.-2C>T	XP_011543301.1:n.-2C>T
XM_024448501.1:c.-2C>T	XP_024304269.1:n.-2C>T
XM_024448502.1:c.-2C>T	XP_024304270.1:n.-2C>T
XM_024448503.1:c.-123C>T	XP_024304271.1:n.-123C>T
XM_024448504.1:c.-2C>T	XP_024304272.1:n.-2C>T
XM_024448505.1:c.-2C>T	XP_024304273.1:n.-2C>T
NM_001567.4:c.-2C>T MANE Select	NP_001558.3:n.-2C>T