Canonical Allele Identifier: CA391690250

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40220697C>G , CM000677.2:g.40220697C>G GRCh38
NC_000015.9:g.40512898C>G , CM000677.1:g.40512898C>G GRCh37
NC_000015.8:g.38300190C>G NCBI36
NG_016338.1:g.64689C>G , LRG_489:g.64689C>G
NG_033169.1:g.8270C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.3091C>G (BUB1B) MANE Select ENSP00000287598.7:p.Leu1031Val
ENST00000453867.7:c.-118+3030C>G (PAK6) ENSP00000401153.3:n.-118+3030C>G
ENST00000558658.6:c.-201+3030C>G (PAK6) ENSP00000456785.2:n.-201+3030C>G
ENST00000287598.10:c.3091C>G (BUB1B) ENSP00000287598.6:p.Leu1031Val
ENST00000412359.7:c.3133C>G (BUB1B) ENSP00000398470.3:p.Leu1045Val
ENST00000441369.6:c.-201+3030C>G (BUB1B-PAK6) ENSP00000406873.1:n.-201+3030C>G
ENST00000453867.6:c.83+3030C>G (BUB1B-PAK6) ENSP00000401153.2:n.83+3030C>G
ENST00000558658.5:c.81+3030C>G (BUB1B-PAK6) ENSP00000456785.1:n.81+3030C>G
ENST00000559435.1:c.197C>G (BUB1B-PAK6)
NM_001128628.2:c.-201+3030C>G (PAK6) NP_001122100.1:n.-201+3030C>G
NM_001128629.2:c.-118+3030C>G (PAK6) NP_001122101.1:n.-118+3030C>G
NM_001211.5:c.3091C>G , LRG_489t1:c.3091C>G (BUB1B) NP_001202.4:p.Leu1031Val
XR_001751506.1:n.217+18788G>C
NM_001128629.3:c.-118+3030C>G (BUB1B-PAK6) NP_001122101.1:n.-118+3030C>G
NM_001211.6:c.3091C>G (BUB1B) MANE Select NP_001202.5:p.Leu1031Val
NM_001128628.3:c.-201+3030C>G (BUB1B-PAK6) NP_001122100.1:n.-201+3030C>G