Canonical Allele Identifier: CA2171676990

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40220787T= , CM000677.2:g.40220787T= GRCh38
NC_000015.9:g.40512988T= , CM000677.1:g.40512988T= GRCh37
NC_000015.8:g.38300280T= NCBI36
NG_016338.1:g.64779T= , LRG_489:g.64779T=
NG_033169.1:g.8360T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.*28T= (BUB1B) MANE Select ENSP00000287598.7:n.*28T=
ENST00000453867.7:c.-118+3120T= (PAK6) ENSP00000401153.3:n.-118+3120T=
ENST00000558658.6:c.-201+3120T= (PAK6) ENSP00000456785.2:n.-201+3120T=
ENST00000287598.10:c.*28T= (BUB1B) ENSP00000287598.6:n.*28T=
ENST00000412359.7:c.*28T= (BUB1B) ENSP00000398470.3:n.*28T=
ENST00000441369.6:c.-201+3120T= (BUB1B-PAK6) ENSP00000406873.1:n.-201+3120T=
ENST00000453867.6:c.83+3120T= (BUB1B-PAK6) ENSP00000401153.2:n.83+3120T=
ENST00000558658.5:c.81+3120T= (BUB1B-PAK6) ENSP00000456785.1:n.81+3120T=
ENST00000559435.1:c.217+70T= (BUB1B-PAK6)
NM_001128628.2:c.-201+3120T= (PAK6) NP_001122100.1:n.-201+3120T=
NM_001128629.2:c.-118+3120T= (PAK6) NP_001122101.1:n.-118+3120T=
NM_001211.5:c.*28T= , LRG_489t1:c.*28T= (BUB1B) NP_001202.4:n.*28T=
XR_001751506.1:n.217+18698A=
NM_001128629.3:c.-118+3120T= (BUB1B-PAK6) NP_001122101.1:n.-118+3120T=
NM_001211.6:c.*28T= (BUB1B) MANE Select NP_001202.5:n.*28T=
NM_001128628.3:c.-201+3120T= (BUB1B-PAK6) NP_001122100.1:n.-201+3120T=