Canonical Allele Identifier: CA2496054092

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806468_47806474delinsATGAATG , CM000664.2:g.47806468_47806474delinsATGAATG	GRCh38
NC_000002.11:g.48033607_48033613delinsATGAATG , CM000664.1:g.48033607_48033613delinsATGAATG	GRCh37
NC_000002.10:g.47887111_47887117delinsATGAATG	NCBI36
NG_007111.1:g.28322_28328delinsATGAATG , LRG_219:g.28322_28328delinsATGAATG
NG_008397.1:g.104202_104208delinsCATTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3521_3527delinsATGAATG (MSH6)	ENSP00000406248.2:p.Asn1174=
ENST00000420813.6:c.3521_3527delinsATGAATG (MSH6)	ENSP00000390382.2:p.Asn1174=
ENST00000455383.6:c.3521_3527delinsATGAATG (MSH6)	ENSP00000397484.2:p.Asn1174=
ENST00000700004.2:c.3434_3440delinsATGAATG (MSH6)	ENSP00000514752.2:p.Asn1145=
ENST00000699999.1:n.4492_4498delinsATGAATG (MSH6)
ENST00000700000.1:c.2252_2258delinsATGAATG (MSH6)	ENSP00000514749.1:p.Asn751=
ENST00000700002.1:c.3824_3830delinsATGAATG (MSH6)	ENSP00000514750.1:p.Asn1275=
ENST00000700003.1:c.1273_1279delinsATGAATG (MSH6)	ENSP00000514751.1:n.1273_1279delinsATGAATG
ENST00000700004.1:c.2591_2597delinsATGAATG (MSH6)	ENSP00000514752.1:p.Asn864=
ENST00000700005.1:n.2669_2675delinsATGAATG (MSH6)
ENST00000700006.1:n.4976_4982delinsATGAATG (MSH6)
ENST00000700007.1:n.2413_2419delinsATGAATG (MSH6)
ENST00000700008.1:n.2080_2086delinsATGAATG (MSH6)
ENST00000700009.1:n.2482_2488delinsATGAATG (MSH6)
ENST00000700010.1:n.1227_1233delinsATGAATG (MSH6)
ENST00000700011.1:n.3112_3118delinsATGAATG (MSH6)
ENST00000682451.1:n.4274_4280delinsCATTCAT (FBXO11)
ENST00000684712.1:n.4536_4542delinsCATTCAT (FBXO11)
ENST00000234420.11:c.3818_3824delinsATGAATG (MSH6) MANE Select	ENSP00000234420.5:p.Asn1273=
ENST00000540021.6:c.3428_3434delinsATGAATG (MSH6)	ENSP00000446475.1:p.Asn1143=
ENST00000652107.1:c.3521_3527delinsATGAATG (MSH6)	ENSP00000498629.1:p.Asn1174=
ENST00000673637.1:c.3521_3527delinsATGAATG (MSH6)	ENSP00000501310.1:p.Asn1174=
ENST00000234420.9:c.3818_3824delinsATGAATG (MSH6)	ENSP00000234420.4:p.Asn1273=
ENST00000405808.5:c.169+1721_169+1727delinsCATTCAT (FBXO11)	ENSP00000385127.1:n.169+1721_169+1727delinsCATTCAT
ENST00000434234.5:c.*124+1520_*124+1526delinsCATTCAT (FBXO11)	ENSP00000402692.1:n.*124+1520_*124+1526delinsCATTCAT
ENST00000445503.5:c.*3165_*3171delinsATGAATG (MSH6)	ENSP00000405294.1:n.*3165_*3171delinsATGAATG
ENST00000538136.1:c.2912_2918delinsATGAATG (MSH6)	ENSP00000438580.1:p.Asn971=
ENST00000540021.5:c.3428_3434delinsATGAATG (MSH6)	ENSP00000446475.1:p.Asn1143=
ENST00000614496.4:c.2912_2918delinsATGAATG (MSH6)	ENSP00000477844.1:p.Asn971=
ENST00000622629.4:c.719_725delinsATGAATG (MSH6)	ENSP00000482078.1:p.Asn240=
NM_000179.2:c.3818_3824delinsATGAATG , LRG_219t1:c.3818_3824delinsATGAATG (MSH6)	NP_000170.1:p.Asn1273=
NM_001281492.1:c.3428_3434delinsATGAATG (MSH6)	NP_001268421.1:p.Asn1143=
NM_001281493.1:c.2912_2918delinsATGAATG (MSH6)	NP_001268422.1:p.Asn971=
NM_001281494.1:c.2912_2918delinsATGAATG (MSH6)	NP_001268423.1:p.Asn971=
XM_005264271.1:c.3521_3527delinsATGAATG (MSH6)	XP_005264328.1:p.Asn1174=
XM_011532798.1:c.3635_3641delinsATGAATG (MSH6)	XP_011531100.1:p.Asn1212=
XM_011532799.1:c.3521_3527delinsATGAATG (MSH6)	XP_011531101.1:p.Asn1174=
XM_011532800.1:c.3521_3527delinsATGAATG (MSH6)	XP_011531102.1:p.Asn1174=
XM_024452819.1:c.3911_3917delinsATGAATG (MSH6)	XP_024308587.1:p.Asn1304=
XM_024452820.1:c.3728_3734delinsATGAATG (MSH6)	XP_024308588.1:p.Asn1243=
XM_024452821.1:c.3614_3620delinsATGAATG (MSH6)	XP_024308589.1:p.Asn1205=
XM_024452822.1:c.3005_3011delinsATGAATG (MSH6)	XP_024308590.1:p.Asn1002=
NM_000179.3:c.3818_3824delinsATGAATG (MSH6) MANE Select	NP_000170.1:p.Asn1273=
NM_001281492.2:c.3428_3434delinsATGAATG (MSH6)	NP_001268421.1:p.Asn1143=
NM_001281493.2:c.2912_2918delinsATGAATG (MSH6)	NP_001268422.1:p.Asn971=
NM_001281494.2:c.2912_2918delinsATGAATG (MSH6)	NP_001268423.1:p.Asn971=