Canonical Allele Identifier: CA2573051983

Gene: FBXO11 MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47808412_47808414del , CM000664.2:g.47808412_47808414del	GRCh38
NC_000002.11:g.48035551_48035553del , CM000664.1:g.48035551_48035553del	GRCh37
NC_000002.10:g.47889055_47889057del	NCBI36
NG_007111.1:g.30266_30268del , LRG_219:g.30266_30268del
NG_008397.1:g.102263_102265del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.6925_6927del (FBXO11)
ENST00000682451.1:n.2416_2418del (FBXO11)
ENST00000682975.1:n.3195_3197del (FBXO11)
ENST00000683894.1:c.2318_2320del (FBXO11)	ENSP00000507789.1:p.Asn773del
ENST00000684085.1:n.5984_5986del (FBXO11)
ENST00000684523.1:n.535_537del (FBXO11)
ENST00000684712.1:n.2678_2680del (FBXO11)
ENST00000403359.8:c.2570_2572del (FBXO11) MANE Select	ENSP00000384823.4:p.Asn857del
ENST00000652107.1:c.*1552_*1554del (MSH6)	ENSP00000498629.1:n.*1552_*1554del
ENST00000234420.9:c.*1552_*1554del (MSH6)	ENSP00000234420.4:n.*1552_*1554del
ENST00000402508.5:c.2318_2320del (FBXO11)	ENSP00000385398.1:p.Asn773del
ENST00000403359.7:c.2570_2572del (FBXO11)	ENSP00000384823.3:p.Asn857del
ENST00000405808.5:c.32_34del (FBXO11)	ENSP00000385127.1:p.Asn11del
ENST00000434234.5:c.32_34del (FBXO11)	ENSP00000402692.1:p.Asn11del
ENST00000465204.5:n.1578_1580del (FBXO11)
NM_001190274.1:c.2570_2572del (FBXO11)	NP_001177203.1:p.Asn857del
NM_025133.4:c.2318_2320del (FBXO11)	NP_079409.3:p.Asn773del
XM_005264572.3:c.2570_2572del (FBXO11)	XP_005264629.1:p.Asn857del
XM_005264573.3:c.2567_2569del (FBXO11)	XP_005264630.1:p.Asn856del
XM_005264572.5:c.2570_2572del (FBXO11)	XP_005264629.1:p.Asn857del
XM_005264573.5:c.2567_2569del (FBXO11)	XP_005264630.1:p.Asn856del
XM_017005015.1:c.2567_2569del (FBXO11)	XP_016860504.1:p.Asn856del
XM_017005016.2:c.2318_2320del (FBXO11)	XP_016860505.1:p.Asn773del
XM_017005017.1:c.2318_2320del (FBXO11)	XP_016860506.1:p.Asn773del
NM_001190274.2:c.2570_2572del (FBXO11) MANE Select	NP_001177203.1:p.Asn857del
NM_001374325.1:c.2318_2320del (FBXO11)	NP_001361254.1:p.Asn773del