Canonical Allele Identifier: CA391689749

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40220622G>A , CM000677.2:g.40220622G>A GRCh38
NC_000015.9:g.40512823G>A , CM000677.1:g.40512823G>A GRCh37
NC_000015.8:g.38300115G>A NCBI36
NG_016338.1:g.64614G>A , LRG_489:g.64614G>A
NG_033169.1:g.8195G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.3016G>A (BUB1B) MANE Select ENSP00000287598.7:p.Glu1006Lys
ENST00000453867.7:c.-118+2955G>A (PAK6) ENSP00000401153.3:n.-118+2955G>A
ENST00000558658.6:c.-201+2955G>A (PAK6) ENSP00000456785.2:n.-201+2955G>A
ENST00000287598.10:c.3016G>A (BUB1B) ENSP00000287598.6:p.Glu1006Lys
ENST00000412359.7:c.3058G>A (BUB1B) ENSP00000398470.3:p.Glu1020Lys
ENST00000441369.6:c.-201+2955G>A (BUB1B-PAK6) ENSP00000406873.1:n.-201+2955G>A
ENST00000453867.6:c.83+2955G>A (BUB1B-PAK6) ENSP00000401153.2:n.83+2955G>A
ENST00000558151.1:n.417G>A (BUB1B)
ENST00000558658.5:c.81+2955G>A (BUB1B-PAK6) ENSP00000456785.1:n.81+2955G>A
ENST00000559435.1:c.122G>A (BUB1B-PAK6)
NM_001128628.2:c.-201+2955G>A (PAK6) NP_001122100.1:n.-201+2955G>A
NM_001128629.2:c.-118+2955G>A (PAK6) NP_001122101.1:n.-118+2955G>A
NM_001211.5:c.3016G>A , LRG_489t1:c.3016G>A (BUB1B) NP_001202.4:p.Glu1006Lys
XR_001751506.1:n.217+18863C>T
NM_001128629.3:c.-118+2955G>A (BUB1B-PAK6) NP_001122101.1:n.-118+2955G>A
NM_001211.6:c.3016G>A (BUB1B) MANE Select NP_001202.5:p.Glu1006Lys
NM_001128628.3:c.-201+2955G>A (BUB1B-PAK6) NP_001122100.1:n.-201+2955G>A