Canonical Allele Identifier: CA381724079
Gene: INPPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1262263936

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72230177C>A , CM000673.2:g.72230177C>A GRCh38
NC_000011.9:g.71941221C>A , CM000673.1:g.71941221C>A GRCh37
NC_000011.8:g.71618869C>A NCBI36
NG_023253.1:g.10340C>A
NG_023253.2:g.10340C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298229.7:c.996C>A MANE Select ENSP00000298229.2:p.Phe332Leu
ENST00000298229.6:c.996C>A ENSP00000298229.2:p.Phe332Leu
ENST00000538751.5:c.270C>A ENSP00000444619.1:p.Phe90Leu
ENST00000540329.5:c.180C>A ENSP00000440018.1:p.Phe60Leu
ENST00000541756.5:c.798C>A ENSP00000446360.2:p.Phe266Leu
NM_001567.3:c.996C>A NP_001558.3:p.Phe332Leu
XM_005273978.3:c.1062C>A XP_005274035.1:p.Phe354Leu
XM_005273979.3:c.1062C>A XP_005274036.1:p.Phe354Leu
XM_011544999.1:c.996C>A XP_011543301.1:p.Phe332Leu
XM_011545000.1:c.1062C>A XP_011543302.1:p.Phe354Leu
XM_005273979.4:c.1062C>A XP_005274036.1:p.Phe354Leu
XM_011544999.2:c.996C>A XP_011543301.1:p.Phe332Leu
XM_024448501.1:c.1062C>A XP_024304269.1:p.Phe354Leu
XM_024448502.1:c.1062C>A XP_024304270.1:p.Phe354Leu
XM_024448503.1:c.1032C>A XP_024304271.1:p.Phe344Leu
XM_024448504.1:c.996C>A XP_024304272.1:p.Phe332Leu
XM_024448505.1:c.1062C>A XP_024304273.1:p.Phe354Leu
NM_001567.4:c.996C>A MANE Select NP_001558.3:p.Phe332Leu