Canonical Allele Identifier: CA346761863
Gene: FBXO11 HGNC NCBI
MSH6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.48035289G>A (hg19) chr2:g.47808150G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47808150G>A , CM000664.2:g.47808150G>A GRCh38
NC_000002.11:g.48035289G>A , CM000664.1:g.48035289G>A GRCh37
NC_000002.10:g.47888793G>A NCBI36
NG_007111.1:g.30004G>A , LRG_219:g.30004G>A
NG_008397.1:g.102526C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681999.1:n.7107C>T (FBXO11)
ENST00000682451.1:n.2598C>T (FBXO11)
ENST00000682975.1:n.3377C>T (FBXO11)
ENST00000683894.1:c.2581C>T (FBXO11) ENSP00000507789.1:p.Pro861Ser
ENST00000684085.1:n.6166C>T (FBXO11)
ENST00000684523.1:n.717C>T (FBXO11)
ENST00000684712.1:n.2860C>T (FBXO11)
ENST00000403359.8:c.2752C>T (FBXO11) MANE Select ENSP00000384823.4:p.Pro918Ser
ENST00000652107.1:c.*1290G>A (MSH6) ENSP00000498629.1:n.*1290G>A
ENST00000234420.9:c.*1290G>A (MSH6) ENSP00000234420.4:n.*1290G>A
ENST00000402508.5:c.2500C>T (FBXO11) ENSP00000385398.1:p.Pro834Ser
ENST00000403359.7:c.2752C>T (FBXO11) ENSP00000384823.3:p.Pro918Ser
ENST00000405808.5:c.169+45C>T (FBXO11) ENSP00000385127.1:n.169+45C>T
ENST00000434234.5:c.214C>T (FBXO11) ENSP00000402692.1:p.Pro72Ser
ENST00000465204.5:n.1760C>T (FBXO11)
NM_001190274.1:c.2752C>T (FBXO11) NP_001177203.1:p.Pro918Ser
NM_025133.4:c.2500C>T (FBXO11) NP_079409.3:p.Pro834Ser
XM_005264572.3:c.2833C>T (FBXO11) XP_005264629.1:p.Pro945Ser
XM_005264573.3:c.2830C>T (FBXO11) XP_005264630.1:p.Pro944Ser
XM_005264572.5:c.2833C>T (FBXO11) XP_005264629.1:p.Pro945Ser
XM_005264573.5:c.2830C>T (FBXO11) XP_005264630.1:p.Pro944Ser
XM_017005015.1:c.2749C>T (FBXO11) XP_016860504.1:p.Pro917Ser
XM_017005016.2:c.2581C>T (FBXO11) XP_016860505.1:p.Pro861Ser
XM_017005017.1:c.2500C>T (FBXO11) XP_016860506.1:p.Pro834Ser
NM_001190274.2:c.2752C>T (FBXO11) MANE Select NP_001177203.1:p.Pro918Ser
NM_001374325.1:c.2500C>T (FBXO11) NP_001361254.1:p.Pro834Ser
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