Canonical Allele Identifier: CA2792650519
Gene: INPPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72225045_72225046del , CM000673.2:g.72225045_72225046del GRCh38
NC_000011.9:g.71936089_71936090del , CM000673.1:g.71936089_71936090del GRCh37
NC_000011.8:g.71613737_71613738del NCBI36
NG_023253.1:g.5208_5209del
NG_023253.2:g.5208_5209del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298229.7:c.61_62del MANE Select ENSP00000298229.2:p.Trp21ValfsTer?
ENST00000298229.6:c.61_62del ENSP00000298229.2:p.Trp21ValfsTer?
ENST00000540973.1:c.61_62del ENSP00000440904.1:p.Trp21ValfsTer?
NM_001567.3:c.61_62del NP_001558.3:p.Trp21ValfsTer?
XM_005273978.3:c.61_62del XP_005274035.1:p.Trp21ValfsTer?
XM_005273979.3:c.61_62del XP_005274036.1:p.Trp21ValfsTer?
XM_011544999.1:c.61_62del XP_011543301.1:p.Trp21ValfsTer?
XM_011545000.1:c.61_62del XP_011543302.1:p.Trp21ValfsTer?
XM_005273979.4:c.61_62del XP_005274036.1:p.Trp21ValfsTer?
XM_011544999.2:c.61_62del XP_011543301.1:p.Trp21ValfsTer?
XM_024448501.1:c.61_62del XP_024304269.1:p.Trp21ValfsTer?
XM_024448502.1:c.61_62del XP_024304270.1:p.Trp21ValfsTer?
XM_024448503.1:c.-61_-60del XP_024304271.1:n.-61_-60del
XM_024448504.1:c.61_62del XP_024304272.1:p.Trp21ValfsTer?
XM_024448505.1:c.61_62del XP_024304273.1:p.Trp21ValfsTer?
NM_001567.4:c.61_62del MANE Select NP_001558.3:p.Trp21ValfsTer?