Canonical Allele Identifier: CA2627774590

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40220836dup , CM000677.2:g.40220836dup GRCh38
NC_000015.9:g.40513037dup , CM000677.1:g.40513037dup GRCh37
NC_000015.8:g.38300329dup NCBI36
NG_016338.1:g.64828dup , LRG_489:g.64828dup
NG_033169.1:g.8409dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000287598.11:c.*77dup (BUB1B) MANE Select ENSP00000287598.7:n.*77dup
ENST00000453867.7:c.-118+3169dup (PAK6) ENSP00000401153.3:n.-118+3169dup
ENST00000558658.6:c.-201+3169dup (PAK6) ENSP00000456785.2:n.-201+3169dup
ENST00000287598.10:c.*77dup (BUB1B) ENSP00000287598.6:n.*77dup
ENST00000412359.7:c.*77dup (BUB1B) ENSP00000398470.3:n.*77dup
ENST00000441369.6:c.-201+3169dup (BUB1B-PAK6) ENSP00000406873.1:n.-201+3169dup
ENST00000453867.6:c.83+3169dup (BUB1B-PAK6) ENSP00000401153.2:n.83+3169dup
ENST00000558658.5:c.81+3169dup (BUB1B-PAK6) ENSP00000456785.1:n.81+3169dup
ENST00000559435.1:c.217+119dup (BUB1B-PAK6)
NM_001128628.2:c.-201+3169dup (PAK6) NP_001122100.1:n.-201+3169dup
NM_001128629.2:c.-118+3169dup (PAK6) NP_001122101.1:n.-118+3169dup
NM_001211.5:c.*77dup , LRG_489t1:c.*77dup (BUB1B) NP_001202.4:n.*77dup
XR_001751506.1:n.217+18649dup
NM_001128629.3:c.-118+3169dup (BUB1B-PAK6) NP_001122101.1:n.-118+3169dup
NM_001211.6:c.*77dup (BUB1B) MANE Select NP_001202.5:n.*77dup
NM_001128628.3:c.-201+3169dup (BUB1B-PAK6) NP_001122100.1:n.-201+3169dup