Canonical Allele Identifier: CA2575676908

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40220465A>T , CM000677.2:g.40220465A>T GRCh38
NC_000015.9:g.40512666A>T , CM000677.1:g.40512666A>T GRCh37
NC_000015.8:g.38299958A>T NCBI36
NG_016338.1:g.64457A>T , LRG_489:g.64457A>T
NG_033169.1:g.8038A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287598.11:c.2958-99A>T (BUB1B) MANE Select ENSP00000287598.7:n.2958-99A>T
ENST00000453867.7:c.-118+2798A>T (PAK6) ENSP00000401153.3:n.-118+2798A>T
ENST00000558658.6:c.-201+2798A>T (PAK6) ENSP00000456785.2:n.-201+2798A>T
ENST00000287598.10:c.2958-99A>T (BUB1B) ENSP00000287598.6:n.2958-99A>T
ENST00000412359.7:c.3000-99A>T (BUB1B) ENSP00000398470.3:n.3000-99A>T
ENST00000441369.6:c.-201+2798A>T (BUB1B-PAK6) ENSP00000406873.1:n.-201+2798A>T
ENST00000453867.6:c.83+2798A>T (BUB1B-PAK6) ENSP00000401153.2:n.83+2798A>T
ENST00000558151.1:n.359-99A>T (BUB1B)
ENST00000558658.5:c.81+2798A>T (BUB1B-PAK6) ENSP00000456785.1:n.81+2798A>T
ENST00000559435.1:c.64-99A>T (BUB1B-PAK6)
NM_001128628.2:c.-201+2798A>T (PAK6) NP_001122100.1:n.-201+2798A>T
NM_001128629.2:c.-118+2798A>T (PAK6) NP_001122101.1:n.-118+2798A>T
NM_001211.5:c.2958-99A>T , LRG_489t1:c.2958-99A>T (BUB1B) NP_001202.4:n.2958-99A>T
XR_001751506.1:n.217+19020T>A
NM_001128629.3:c.-118+2798A>T (BUB1B-PAK6) NP_001122101.1:n.-118+2798A>T
NM_001211.6:c.2958-99A>T (BUB1B) MANE Select NP_001202.5:n.2958-99A>T
NM_001128628.3:c.-201+2798A>T (BUB1B-PAK6) NP_001122100.1:n.-201+2798A>T