Canonical Allele Identifier: CA2171676729

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40220152G= , CM000677.2:g.40220152G= GRCh38
NC_000015.9:g.40512353G= , CM000677.1:g.40512353G= GRCh37
NC_000015.8:g.38299645G= NCBI36
NG_016338.1:g.64144G= , LRG_489:g.64144G=
NG_033169.1:g.7725G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.2958-412G= (BUB1B) MANE Select ENSP00000287598.7:n.2958-412G=
ENST00000453867.7:c.-118+2485G= (PAK6) ENSP00000401153.3:n.-118+2485G=
ENST00000558658.6:c.-201+2485G= (PAK6) ENSP00000456785.2:n.-201+2485G=
ENST00000287598.10:c.2958-412G= (BUB1B) ENSP00000287598.6:n.2958-412G=
ENST00000412359.7:c.3000-412G= (BUB1B) ENSP00000398470.3:n.3000-412G=
ENST00000441369.6:c.-201+2485G= (BUB1B-PAK6) ENSP00000406873.1:n.-201+2485G=
ENST00000453867.6:c.83+2485G= (BUB1B-PAK6) ENSP00000401153.2:n.83+2485G=
ENST00000558151.1:n.359-412G= (BUB1B)
ENST00000558658.5:c.81+2485G= (BUB1B-PAK6) ENSP00000456785.1:n.81+2485G=
ENST00000559435.1:c.64-412G= (BUB1B-PAK6)
NM_001128628.2:c.-201+2485G= (PAK6) NP_001122100.1:n.-201+2485G=
NM_001128629.2:c.-118+2485G= (PAK6) NP_001122101.1:n.-118+2485G=
NM_001211.5:c.2958-412G= , LRG_489t1:c.2958-412G= (BUB1B) NP_001202.4:n.2958-412G=
XR_001751506.1:n.217+19333C=
NM_001128629.3:c.-118+2485G= (BUB1B-PAK6) NP_001122101.1:n.-118+2485G=
NM_001211.6:c.2958-412G= (BUB1B) MANE Select NP_001202.5:n.2958-412G=
NM_001128628.3:c.-201+2485G= (BUB1B-PAK6) NP_001122100.1:n.-201+2485G=