Canonical Allele Identifier: CA2658967983

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806416-C-CTAGCACATGTATCGCTAATA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806418_47806437dup , CM000664.2:g.47806418_47806437dup	GRCh38
NC_000002.11:g.48033557_48033576dup , CM000664.1:g.48033557_48033576dup	GRCh37
NC_000002.10:g.47887061_47887080dup	NCBI36
NG_007111.1:g.28272_28291dup , LRG_219:g.28272_28291dup
NG_008397.1:g.104240_104259dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3505-34_3505-15dup (MSH6)	ENSP00000406248.2:n.3505-34_3505-15dup
ENST00000420813.6:c.3505-34_3505-15dup (MSH6)	ENSP00000390382.2:n.3505-34_3505-15dup
ENST00000455383.6:c.3505-34_3505-15dup (MSH6)	ENSP00000397484.2:n.3505-34_3505-15dup
ENST00000700004.2:c.3418-34_3418-15dup (MSH6)	ENSP00000514752.2:n.3418-34_3418-15dup
ENST00000699999.1:n.4476-34_4476-15dup (MSH6)
ENST00000700000.1:c.2236-34_2236-15dup (MSH6)	ENSP00000514749.1:n.2236-34_2236-15dup
ENST00000700002.1:c.3808-34_3808-15dup (MSH6)	ENSP00000514750.1:n.3808-34_3808-15dup
ENST00000700003.1:c.1257-34_1257-15dup (MSH6)	ENSP00000514751.1:n.1257-34_1257-15dup
ENST00000700004.1:c.2575-34_2575-15dup (MSH6)	ENSP00000514752.1:n.2575-34_2575-15dup
ENST00000700005.1:n.2653-34_2653-15dup (MSH6)
ENST00000700006.1:n.4960-34_4960-15dup (MSH6)
ENST00000700007.1:n.2397-34_2397-15dup (MSH6)
ENST00000700008.1:n.2030_2049dup (MSH6)
ENST00000700009.1:n.2466-34_2466-15dup (MSH6)
ENST00000700010.1:n.1211-34_1211-15dup (MSH6)
ENST00000700011.1:n.3096-34_3096-15dup (MSH6)
ENST00000682451.1:n.4312_4331dup (FBXO11)
ENST00000684712.1:n.4574_4593dup (FBXO11)
ENST00000234420.11:c.3802-34_3802-15dup (MSH6) MANE Select	ENSP00000234420.5:n.3802-34_3802-15dup
ENST00000540021.6:c.3412-34_3412-15dup (MSH6)	ENSP00000446475.1:n.3412-34_3412-15dup
ENST00000652107.1:c.3505-34_3505-15dup (MSH6)	ENSP00000498629.1:n.3505-34_3505-15dup
ENST00000673637.1:c.3505-34_3505-15dup (MSH6)	ENSP00000501310.1:n.3505-34_3505-15dup
ENST00000234420.9:c.3802-34_3802-15dup (MSH6)	ENSP00000234420.4:n.3802-34_3802-15dup
ENST00000405808.5:c.169+1759_169+1778dup (FBXO11)	ENSP00000385127.1:n.169+1759_169+1778dup
ENST00000434234.5:c.*124+1558_*124+1577dup (FBXO11)	ENSP00000402692.1:n.*124+1558_*124+1577dup
ENST00000445503.5:c.*3149-34_*3149-15dup (MSH6)	ENSP00000405294.1:n.*3149-34_*3149-15dup
ENST00000538136.1:c.2896-34_2896-15dup (MSH6)	ENSP00000438580.1:n.2896-34_2896-15dup
ENST00000540021.5:c.3412-34_3412-15dup (MSH6)	ENSP00000446475.1:n.3412-34_3412-15dup
ENST00000614496.4:c.2896-34_2896-15dup (MSH6)	ENSP00000477844.1:n.2896-34_2896-15dup
ENST00000622629.4:c.703-34_703-15dup (MSH6)	ENSP00000482078.1:n.703-34_703-15dup
NM_000179.2:c.3802-34_3802-15dup , LRG_219t1:c.3802-34_3802-15dup (MSH6)	NP_000170.1:n.3802-34_3802-15dup
NM_001281492.1:c.3412-34_3412-15dup (MSH6)	NP_001268421.1:n.3412-34_3412-15dup
NM_001281493.1:c.2896-34_2896-15dup (MSH6)	NP_001268422.1:n.2896-34_2896-15dup
NM_001281494.1:c.2896-34_2896-15dup (MSH6)	NP_001268423.1:n.2896-34_2896-15dup
XM_005264271.1:c.3505-34_3505-15dup (MSH6)	XP_005264328.1:n.3505-34_3505-15dup
XM_011532798.1:c.3619-34_3619-15dup (MSH6)	XP_011531100.1:n.3619-34_3619-15dup
XM_011532799.1:c.3505-34_3505-15dup (MSH6)	XP_011531101.1:n.3505-34_3505-15dup
XM_011532800.1:c.3505-34_3505-15dup (MSH6)	XP_011531102.1:n.3505-34_3505-15dup
XM_024452819.1:c.3861_3880dup (MSH6)	XP_024308587.1:p.Phe1294Ter
XM_024452820.1:c.3678_3697dup (MSH6)	XP_024308588.1:p.Phe1233Ter
XM_024452821.1:c.3564_3583dup (MSH6)	XP_024308589.1:p.Phe1195Ter
XM_024452822.1:c.2955_2974dup (MSH6)	XP_024308590.1:p.Phe992Ter
NM_000179.3:c.3802-34_3802-15dup (MSH6) MANE Select	NP_000170.1:n.3802-34_3802-15dup
NM_001281492.2:c.3412-34_3412-15dup (MSH6)	NP_001268421.1:n.3412-34_3412-15dup
NM_001281493.2:c.2896-34_2896-15dup (MSH6)	NP_001268422.1:n.2896-34_2896-15dup
NM_001281494.2:c.2896-34_2896-15dup (MSH6)	NP_001268423.1:n.2896-34_2896-15dup