Canonical Allele Identifier: CA2496054090

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806468A= , CM000664.2:g.47806468A=	GRCh38
NC_000002.11:g.48033607A= , CM000664.1:g.48033607A=	GRCh37
NC_000002.10:g.47887111A=	NCBI36
NG_007111.1:g.28322A= , LRG_219:g.28322A=
NG_008397.1:g.104208T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3521A= (MSH6)	ENSP00000406248.2:p.Asn1174=
ENST00000420813.6:c.3521A= (MSH6)	ENSP00000390382.2:p.Asn1174=
ENST00000455383.6:c.3521A= (MSH6)	ENSP00000397484.2:p.Asn1174=
ENST00000700004.2:c.3434A= (MSH6)	ENSP00000514752.2:p.Asn1145=
ENST00000699999.1:n.4492A= (MSH6)
ENST00000700000.1:c.2252A= (MSH6)	ENSP00000514749.1:p.Asn751=
ENST00000700002.1:c.3824A= (MSH6)	ENSP00000514750.1:p.Asn1275=
ENST00000700003.1:c.1273A= (MSH6)	ENSP00000514751.1:n.1273A=
ENST00000700004.1:c.2591A= (MSH6)	ENSP00000514752.1:p.Asn864=
ENST00000700005.1:n.2669A= (MSH6)
ENST00000700006.1:n.4976A= (MSH6)
ENST00000700007.1:n.2413A= (MSH6)
ENST00000700008.1:n.2080A= (MSH6)
ENST00000700009.1:n.2482A= (MSH6)
ENST00000700010.1:n.1227A= (MSH6)
ENST00000700011.1:n.3112A= (MSH6)
ENST00000682451.1:n.4280T= (FBXO11)
ENST00000684712.1:n.4542T= (FBXO11)
ENST00000234420.11:c.3818A= (MSH6) MANE Select	ENSP00000234420.5:p.Asn1273=
ENST00000540021.6:c.3428A= (MSH6)	ENSP00000446475.1:p.Asn1143=
ENST00000652107.1:c.3521A= (MSH6)	ENSP00000498629.1:p.Asn1174=
ENST00000673637.1:c.3521A= (MSH6)	ENSP00000501310.1:p.Asn1174=
ENST00000234420.9:c.3818A= (MSH6)	ENSP00000234420.4:p.Asn1273=
ENST00000405808.5:c.169+1727T= (FBXO11)	ENSP00000385127.1:n.169+1727T=
ENST00000434234.5:c.*124+1526T= (FBXO11)	ENSP00000402692.1:n.*124+1526T=
ENST00000445503.5:c.*3165A= (MSH6)	ENSP00000405294.1:n.*3165A=
ENST00000538136.1:c.2912A= (MSH6)	ENSP00000438580.1:p.Asn971=
ENST00000540021.5:c.3428A= (MSH6)	ENSP00000446475.1:p.Asn1143=
ENST00000614496.4:c.2912A= (MSH6)	ENSP00000477844.1:p.Asn971=
ENST00000622629.4:c.719A= (MSH6)	ENSP00000482078.1:p.Asn240=
NM_000179.2:c.3818A= , LRG_219t1:c.3818A= (MSH6)	NP_000170.1:p.Asn1273=
NM_001281492.1:c.3428A= (MSH6)	NP_001268421.1:p.Asn1143=
NM_001281493.1:c.2912A= (MSH6)	NP_001268422.1:p.Asn971=
NM_001281494.1:c.2912A= (MSH6)	NP_001268423.1:p.Asn971=
XM_005264271.1:c.3521A= (MSH6)	XP_005264328.1:p.Asn1174=
XM_011532798.1:c.3635A= (MSH6)	XP_011531100.1:p.Asn1212=
XM_011532799.1:c.3521A= (MSH6)	XP_011531101.1:p.Asn1174=
XM_011532800.1:c.3521A= (MSH6)	XP_011531102.1:p.Asn1174=
XM_024452819.1:c.3911A= (MSH6)	XP_024308587.1:p.Asn1304=
XM_024452820.1:c.3728A= (MSH6)	XP_024308588.1:p.Asn1243=
XM_024452821.1:c.3614A= (MSH6)	XP_024308589.1:p.Asn1205=
XM_024452822.1:c.3005A= (MSH6)	XP_024308590.1:p.Asn1002=
NM_000179.3:c.3818A= (MSH6) MANE Select	NP_000170.1:p.Asn1273=
NM_001281492.2:c.3428A= (MSH6)	NP_001268421.1:p.Asn1143=
NM_001281493.2:c.2912A= (MSH6)	NP_001268422.1:p.Asn971=
NM_001281494.2:c.2912A= (MSH6)	NP_001268423.1:p.Asn971=