Canonical Allele Identifier: CA2586964954

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804994dup , CM000664.2:g.47804994dup	GRCh38
NC_000002.11:g.48032133dup , CM000664.1:g.48032133dup	GRCh37
NC_000002.10:g.47885637dup	NCBI36
NG_007111.1:g.26848dup , LRG_219:g.26848dup
NG_008397.1:g.105682dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3226dup (MSH6)	ENSP00000406248.2:p.Thr1076AsnfsTer2
ENST00000420813.6:c.3226dup (MSH6)	ENSP00000390382.2:p.Thr1076AsnfsTer2
ENST00000455383.6:c.3226dup (MSH6)	ENSP00000397484.2:p.Thr1076AsnfsTer2
ENST00000700004.2:c.3173-624dup (MSH6)	ENSP00000514752.2:n.3173-624dup
ENST00000699999.1:n.3607dup (MSH6)
ENST00000700000.1:c.1957dup (MSH6)	ENSP00000514749.1:p.Thr653AsnfsTer2
ENST00000700002.1:c.3529dup (MSH6)	ENSP00000514750.1:p.Thr1177AsnfsTer2
ENST00000700003.1:c.978dup (MSH6)	ENSP00000514751.1:n.978dup
ENST00000700004.1:c.2330-624dup (MSH6)	ENSP00000514752.1:n.2330-624dup
ENST00000700005.1:n.2374dup (MSH6)
ENST00000700006.1:n.3595dup (MSH6)
ENST00000700007.1:n.1528dup (MSH6)
ENST00000700008.1:n.1102dup (MSH6)
ENST00000700009.1:n.1101dup (MSH6)
ENST00000700010.1:n.932dup (MSH6)
ENST00000700011.1:n.2227dup (MSH6)
ENST00000234420.11:c.3523dup (MSH6) MANE Select	ENSP00000234420.5:p.Thr1175AsnfsTer2
ENST00000540021.6:c.3133dup (MSH6)	ENSP00000446475.1:p.Thr1045AsnfsTer2
ENST00000652107.1:c.3226dup (MSH6)	ENSP00000498629.1:p.Thr1076AsnfsTer2
ENST00000673637.1:c.3226dup (MSH6)	ENSP00000501310.1:p.Thr1076AsnfsTer2
ENST00000234420.9:c.3523dup (MSH6)	ENSP00000234420.4:p.Thr1175AsnfsTer2
ENST00000405808.5:c.169+3201dup (FBXO11)	ENSP00000385127.1:n.169+3201dup
ENST00000434234.5:c.*124+3000dup (FBXO11)	ENSP00000402692.1:n.*124+3000dup
ENST00000445503.5:c.*2870dup (MSH6)	ENSP00000405294.1:n.*2870dup
ENST00000538136.1:c.2617dup (MSH6)	ENSP00000438580.1:p.Thr873AsnfsTer2
ENST00000540021.5:c.3133dup (MSH6)	ENSP00000446475.1:p.Thr1045AsnfsTer2
ENST00000614496.4:c.2617dup (MSH6)	ENSP00000477844.1:p.Thr873AsnfsTer2
ENST00000622629.4:c.427dup (MSH6)	ENSP00000482078.1:p.Thr143AsnfsTer2
NM_000179.2:c.3523dup , LRG_219t1:c.3523dup (MSH6)	NP_000170.1:p.Thr1175AsnfsTer2
NM_001281492.1:c.3133dup (MSH6)	NP_001268421.1:p.Thr1045AsnfsTer2
NM_001281493.1:c.2617dup (MSH6)	NP_001268422.1:p.Thr873AsnfsTer2
NM_001281494.1:c.2617dup (MSH6)	NP_001268423.1:p.Thr873AsnfsTer2
XM_005264271.1:c.3226dup (MSH6)	XP_005264328.1:p.Thr1076AsnfsTer2
XM_011532798.1:c.3340dup (MSH6)	XP_011531100.1:p.Thr1114AsnfsTer2
XM_011532799.1:c.3226dup (MSH6)	XP_011531101.1:p.Thr1076AsnfsTer2
XM_011532800.1:c.3226dup (MSH6)	XP_011531102.1:p.Thr1076AsnfsTer2
XM_024452819.1:c.3523dup (MSH6)	XP_024308587.1:p.Thr1175AsnfsTer2
XM_024452820.1:c.3340dup (MSH6)	XP_024308588.1:p.Thr1114AsnfsTer2
XM_024452821.1:c.3226dup (MSH6)	XP_024308589.1:p.Thr1076AsnfsTer2
XM_024452822.1:c.2617dup (MSH6)	XP_024308590.1:p.Thr873AsnfsTer2
NM_000179.3:c.3523dup (MSH6) MANE Select	NP_000170.1:p.Thr1175AsnfsTer2
NM_001281492.2:c.3133dup (MSH6)	NP_001268421.1:p.Thr1045AsnfsTer2
NM_001281493.2:c.2617dup (MSH6)	NP_001268422.1:p.Thr873AsnfsTer2
NM_001281494.2:c.2617dup (MSH6)	NP_001268423.1:p.Thr873AsnfsTer2