Canonical Allele Identifier: CA1030298319

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806929_47806964dup , CM000664.2:g.47806929_47806964dup GRCh38
NC_000002.11:g.48034068_48034103dup , CM000664.1:g.48034068_48034103dup GRCh37
NC_000002.10:g.47887572_47887607dup NCBI36
NG_007111.1:g.28783_28818dup , LRG_219:g.28783_28818dup
NG_008397.1:g.103712_103747dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682451.1:n.3784_3819dup (FBXO11)
ENST00000684712.1:n.4046_4081dup (FBXO11)
ENST00000403359.8:c.*1154_*1189dup (FBXO11) MANE Select ENSP00000384823.4:n.*1154_*1189dup
ENST00000652107.1:c.*69_*104dup (MSH6) ENSP00000498629.1:n.*69_*104dup
ENST00000234420.9:c.*69_*104dup (MSH6) ENSP00000234420.4:n.*69_*104dup
ENST00000402508.5:c.*1154_*1189dup (FBXO11) ENSP00000385398.1:n.*1154_*1189dup
ENST00000403359.7:c.*1154_*1189dup (FBXO11) ENSP00000384823.3:n.*1154_*1189dup
ENST00000405808.5:c.169+1231_169+1266dup (FBXO11) ENSP00000385127.1:n.169+1231_169+1266dup
ENST00000434234.5:c.*124+1030_*124+1065dup (FBXO11) ENSP00000402692.1:n.*124+1030_*124+1065dup
ENST00000465204.5:n.2946_2981dup (FBXO11)
NM_001190274.1:c.*1154_*1189dup (FBXO11) NP_001177203.1:n.*1154_*1189dup
NM_025133.4:c.*1154_*1189dup (FBXO11) NP_079409.3:n.*1154_*1189dup
XM_005264572.3:c.*1154_*1189dup (FBXO11) XP_005264629.1:n.*1154_*1189dup
XM_005264573.3:c.*1154_*1189dup (FBXO11) XP_005264630.1:n.*1154_*1189dup
XM_005264572.5:c.*1154_*1189dup (FBXO11) XP_005264629.1:n.*1154_*1189dup
XM_005264573.5:c.*1154_*1189dup (FBXO11) XP_005264630.1:n.*1154_*1189dup
XM_017005015.1:c.*1154_*1189dup (FBXO11) XP_016860504.1:n.*1154_*1189dup
XM_017005016.2:c.*1154_*1189dup (FBXO11) XP_016860505.1:n.*1154_*1189dup
XM_017005017.1:c.*1154_*1189dup (FBXO11) XP_016860506.1:n.*1154_*1189dup
NM_001190274.2:c.*1154_*1189dup (FBXO11) MANE Select NP_001177203.1:n.*1154_*1189dup
NM_001374325.1:c.*1154_*1189dup (FBXO11) NP_001361254.1:n.*1154_*1189dup