Canonical Allele Identifier: CA2586969245

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799289_47799290dup , CM000664.2:g.47799289_47799290dup	GRCh38
NC_000002.11:g.48026428_48026429dup , CM000664.1:g.48026428_48026429dup	GRCh37
NC_000002.10:g.47879932_47879933dup	NCBI36
NG_007111.1:g.21143_21144dup , LRG_219:g.21143_21144dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.1009_1010dup (MSH6)	ENSP00000406248.2:p.His338ThrfsTer17
ENST00000420813.6:c.1009_1010dup (MSH6)	ENSP00000390382.2:p.His338ThrfsTer17
ENST00000455383.6:c.1009_1010dup (MSH6)	ENSP00000397484.2:p.His338ThrfsTer17
ENST00000700004.2:c.1306_1307dup (MSH6)	ENSP00000514752.2:p.His437ThrfsTer17
ENST00000699999.1:n.1390_1391dup (MSH6)
ENST00000700000.1:c.1306_1307dup (MSH6)	ENSP00000514749.1:p.His437ThrfsTer17
ENST00000700002.1:c.1312_1313dup (MSH6)	ENSP00000514750.1:p.His439ThrfsTer17
ENST00000700003.1:c.627+3226_627+3227dup (MSH6)	ENSP00000514751.1:n.627+3226_627+3227dup
ENST00000700004.1:c.463_464dup (MSH6)	ENSP00000514752.1:p.His156ThrfsTer17
ENST00000234420.11:c.1306_1307dup (MSH6) MANE Select	ENSP00000234420.5:p.His437ThrfsTer17
ENST00000540021.6:c.916_917dup (MSH6)	ENSP00000446475.1:p.His307ThrfsTer17
ENST00000652107.1:c.1009_1010dup (MSH6)	ENSP00000498629.1:p.His338ThrfsTer17
ENST00000673637.1:c.1009_1010dup (MSH6)	ENSP00000501310.1:p.His338ThrfsTer17
ENST00000234420.9:c.1306_1307dup (MSH6)	ENSP00000234420.4:p.His437ThrfsTer17
ENST00000405808.5:c.169+8905_169+8906dup (FBXO11)	ENSP00000385127.1:n.169+8905_169+8906dup
ENST00000434234.5:c.*124+8704_*124+8705dup (FBXO11)	ENSP00000402692.1:n.*124+8704_*124+8705dup
ENST00000445503.5:c.*653_*654dup (MSH6)	ENSP00000405294.1:n.*653_*654dup
ENST00000538136.1:c.400_401dup (MSH6)	ENSP00000438580.1:p.His135ThrfsTer17
ENST00000540021.5:c.916_917dup (MSH6)	ENSP00000446475.1:p.His307ThrfsTer17
ENST00000614496.4:c.400_401dup (MSH6)	ENSP00000477844.1:p.His135ThrfsTer17
ENST00000616033.4:c.1303_1304dup (MSH6)	ENSP00000480261.1:p.His436ThrfsTer17
ENST00000622629.4:c.-1791_-1790dup (MSH6)	ENSP00000482078.1:n.-1791_-1790dup
NM_000179.2:c.1306_1307dup , LRG_219t1:c.1306_1307dup (MSH6)	NP_000170.1:p.His437ThrfsTer17
NM_001281492.1:c.916_917dup (MSH6)	NP_001268421.1:p.His307ThrfsTer17
NM_001281493.1:c.400_401dup (MSH6)	NP_001268422.1:p.His135ThrfsTer17
NM_001281494.1:c.400_401dup (MSH6)	NP_001268423.1:p.His135ThrfsTer17
XM_005264271.1:c.1009_1010dup (MSH6)	XP_005264328.1:p.His338ThrfsTer17
XM_011532798.1:c.1123_1124dup (MSH6)	XP_011531100.1:p.His376ThrfsTer17
XM_011532799.1:c.1009_1010dup (MSH6)	XP_011531101.1:p.His338ThrfsTer17
XM_011532800.1:c.1009_1010dup (MSH6)	XP_011531102.1:p.His338ThrfsTer17
XM_024452819.1:c.1306_1307dup (MSH6)	XP_024308587.1:p.His437ThrfsTer17
XM_024452820.1:c.1123_1124dup (MSH6)	XP_024308588.1:p.His376ThrfsTer17
XM_024452821.1:c.1009_1010dup (MSH6)	XP_024308589.1:p.His338ThrfsTer17
XM_024452822.1:c.400_401dup (MSH6)	XP_024308590.1:p.His135ThrfsTer17
NM_000179.3:c.1306_1307dup (MSH6) MANE Select	NP_000170.1:p.His437ThrfsTer17
NM_001281492.2:c.916_917dup (MSH6)	NP_001268421.1:p.His307ThrfsTer17
NM_001281493.2:c.400_401dup (MSH6)	NP_001268422.1:p.His135ThrfsTer17
NM_001281494.2:c.400_401dup (MSH6)	NP_001268423.1:p.His135ThrfsTer17