Canonical Allele Identifier: CA776271
Community Standard Title: NM_005540.3(INPP5B):c.486dup (p.Asn163Ter)
Gene: INPP5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.37931959dup , CM000663.2:g.37931959dup GRCh38
NC_000001.10:g.38397631dup , CM000663.1:g.38397631dup GRCh37
NC_000001.9:g.38170218dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_005540.3:c.486dup MANE Select NP_005531.2:p.Asn163Ter
ENST00000373024.8:c.486dup MANE Select ENSP00000362115.3:p.Asn163Ter
NM_001350228.1:c.-241dup NP_001337157.1:n.-241dup
NM_001365820.1:c.486dup NP_001352749.1:p.Asn163Ter
NM_001365821.1:c.480dup NP_001352750.1:p.Asn161Ter
NM_001365822.1:c.420dup NP_001352751.1:p.Asn141Ter
NM_001365823.1:c.291dup NP_001352752.1:p.Asn98Ter
NM_001365824.1:c.291dup NP_001352753.1:p.Asn98Ter
NM_001365825.1:c.129dup NP_001352754.1:p.Asn44Ter
NM_005540.2:c.486dup NP_005531.2:p.Asn163Ter
NR_158628.1:n.759dup
NR_158629.1:n.762dup
NR_158630.1:n.580dup
ENST00000373021.1:c.486dup ENSP00000362112.1:p.Asn163Ter
ENST00000373023.6:c.486dup ENSP00000362114.2:p.Asn163Ter
ENST00000373024.7:c.486dup ENSP00000362115.3:p.Asn163Ter
ENST00000373026.5:c.486dup ENSP00000362117.1:p.Asn163Ter
ENST00000458109.6:c.486dup ENSP00000397748.3:p.Asn163Ter
XM_005270835.3:c.486dup XP_005270892.1:p.Asn163Ter
XM_006710621.2:c.291dup XP_006710684.2:p.Asn98Ter
XM_011541387.1:c.420dup XP_011539689.1:p.Asn141Ter
XM_011541388.1:c.390dup XP_011539690.1:p.Asn131Ter
XM_011541389.1:c.486dup XP_011539691.1:p.Asn163Ter
XM_011541390.1:c.486dup XP_011539692.1:p.Asn163Ter
XM_011541391.1:c.486dup XP_011539693.1:p.Asn163Ter
XM_011541392.1:c.-98dup XP_011539694.1:n.-98dup
XM_011541392.2:c.-98dup XP_011539694.1:n.-98dup
XM_011541393.1:c.-74dup XP_011539695.1:n.-74dup
XM_011541393.2:c.-74dup XP_011539695.1:n.-74dup
XM_017001206.1:c.486dup XP_016856695.1:p.Asn163Ter
XM_024446762.1:c.486dup XP_024302530.1:p.Asn163Ter
XR_946643.1:n.607dup
XR_946643.2:n.617dup
XR_946644.1:n.607dup
XR_946644.3:n.618dup