Canonical Allele Identifier: CA391690192

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40220683C>A , CM000677.2:g.40220683C>A GRCh38
NC_000015.9:g.40512884C>A , CM000677.1:g.40512884C>A GRCh37
NC_000015.8:g.38300176C>A NCBI36
NG_016338.1:g.64675C>A , LRG_489:g.64675C>A
NG_033169.1:g.8256C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.3077C>A (BUB1B) MANE Select ENSP00000287598.7:p.Thr1026Lys
ENST00000453867.7:c.-118+3016C>A (PAK6) ENSP00000401153.3:n.-118+3016C>A
ENST00000558658.6:c.-201+3016C>A (PAK6) ENSP00000456785.2:n.-201+3016C>A
ENST00000287598.10:c.3077C>A (BUB1B) ENSP00000287598.6:p.Thr1026Lys
ENST00000412359.7:c.3119C>A (BUB1B) ENSP00000398470.3:p.Thr1040Lys
ENST00000441369.6:c.-201+3016C>A (BUB1B-PAK6) ENSP00000406873.1:n.-201+3016C>A
ENST00000453867.6:c.83+3016C>A (BUB1B-PAK6) ENSP00000401153.2:n.83+3016C>A
ENST00000558658.5:c.81+3016C>A (BUB1B-PAK6) ENSP00000456785.1:n.81+3016C>A
ENST00000559435.1:c.183C>A (BUB1B-PAK6)
NM_001128628.2:c.-201+3016C>A (PAK6) NP_001122100.1:n.-201+3016C>A
NM_001128629.2:c.-118+3016C>A (PAK6) NP_001122101.1:n.-118+3016C>A
NM_001211.5:c.3077C>A , LRG_489t1:c.3077C>A (BUB1B) NP_001202.4:p.Thr1026Lys
XR_001751506.1:n.217+18802G>T
NM_001128629.3:c.-118+3016C>A (BUB1B-PAK6) NP_001122101.1:n.-118+3016C>A
NM_001211.6:c.3077C>A (BUB1B) MANE Select NP_001202.5:p.Thr1026Lys
NM_001128628.3:c.-201+3016C>A (BUB1B-PAK6) NP_001122100.1:n.-201+3016C>A