Canonical Allele Identifier: CA2658967988

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806434-A-ATAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806436_47806438dup , CM000664.2:g.47806436_47806438dup	GRCh38
NC_000002.11:g.48033575_48033577dup , CM000664.1:g.48033575_48033577dup	GRCh37
NC_000002.10:g.47887079_47887081dup	NCBI36
NG_007111.1:g.28290_28292dup , LRG_219:g.28290_28292dup
NG_008397.1:g.104239_104241dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3505-16_3505-14dup (MSH6)	ENSP00000406248.2:n.3505-16_3505-14dup
ENST00000420813.6:c.3505-16_3505-14dup (MSH6)	ENSP00000390382.2:n.3505-16_3505-14dup
ENST00000455383.6:c.3505-16_3505-14dup (MSH6)	ENSP00000397484.2:n.3505-16_3505-14dup
ENST00000700004.2:c.3418-16_3418-14dup (MSH6)	ENSP00000514752.2:n.3418-16_3418-14dup
ENST00000699999.1:n.4476-16_4476-14dup (MSH6)
ENST00000700000.1:c.2236-16_2236-14dup (MSH6)	ENSP00000514749.1:n.2236-16_2236-14dup
ENST00000700002.1:c.3808-16_3808-14dup (MSH6)	ENSP00000514750.1:n.3808-16_3808-14dup
ENST00000700003.1:c.1257-16_1257-14dup (MSH6)	ENSP00000514751.1:n.1257-16_1257-14dup
ENST00000700004.1:c.2575-16_2575-14dup (MSH6)	ENSP00000514752.1:n.2575-16_2575-14dup
ENST00000700005.1:n.2653-16_2653-14dup (MSH6)
ENST00000700006.1:n.4960-16_4960-14dup (MSH6)
ENST00000700007.1:n.2397-16_2397-14dup (MSH6)
ENST00000700008.1:n.2048_2050dup (MSH6)
ENST00000700009.1:n.2466-16_2466-14dup (MSH6)
ENST00000700010.1:n.1211-16_1211-14dup (MSH6)
ENST00000700011.1:n.3096-16_3096-14dup (MSH6)
ENST00000682451.1:n.4311_4313dup (FBXO11)
ENST00000684712.1:n.4573_4575dup (FBXO11)
ENST00000234420.11:c.3802-16_3802-14dup (MSH6) MANE Select	ENSP00000234420.5:n.3802-16_3802-14dup
ENST00000540021.6:c.3412-16_3412-14dup (MSH6)	ENSP00000446475.1:n.3412-16_3412-14dup
ENST00000652107.1:c.3505-16_3505-14dup (MSH6)	ENSP00000498629.1:n.3505-16_3505-14dup
ENST00000673637.1:c.3505-16_3505-14dup (MSH6)	ENSP00000501310.1:n.3505-16_3505-14dup
ENST00000234420.9:c.3802-16_3802-14dup (MSH6)	ENSP00000234420.4:n.3802-16_3802-14dup
ENST00000405808.5:c.169+1758_169+1760dup (FBXO11)	ENSP00000385127.1:n.169+1758_169+1760dup
ENST00000434234.5:c.*124+1557_*124+1559dup (FBXO11)	ENSP00000402692.1:n.*124+1557_*124+1559dup
ENST00000445503.5:c.*3149-16_*3149-14dup (MSH6)	ENSP00000405294.1:n.*3149-16_*3149-14dup
ENST00000538136.1:c.2896-16_2896-14dup (MSH6)	ENSP00000438580.1:n.2896-16_2896-14dup
ENST00000540021.5:c.3412-16_3412-14dup (MSH6)	ENSP00000446475.1:n.3412-16_3412-14dup
ENST00000614496.4:c.2896-16_2896-14dup (MSH6)	ENSP00000477844.1:n.2896-16_2896-14dup
ENST00000622629.4:c.703-16_703-14dup (MSH6)	ENSP00000482078.1:n.703-16_703-14dup
NM_000179.2:c.3802-16_3802-14dup , LRG_219t1:c.3802-16_3802-14dup (MSH6)	NP_000170.1:n.3802-16_3802-14dup
NM_001281492.1:c.3412-16_3412-14dup (MSH6)	NP_001268421.1:n.3412-16_3412-14dup
NM_001281493.1:c.2896-16_2896-14dup (MSH6)	NP_001268422.1:n.2896-16_2896-14dup
NM_001281494.1:c.2896-16_2896-14dup (MSH6)	NP_001268423.1:n.2896-16_2896-14dup
XM_005264271.1:c.3505-16_3505-14dup (MSH6)	XP_005264328.1:n.3505-16_3505-14dup
XM_011532798.1:c.3619-16_3619-14dup (MSH6)	XP_011531100.1:n.3619-16_3619-14dup
XM_011532799.1:c.3505-16_3505-14dup (MSH6)	XP_011531101.1:n.3505-16_3505-14dup
XM_011532800.1:c.3505-16_3505-14dup (MSH6)	XP_011531102.1:n.3505-16_3505-14dup
XM_024452819.1:c.3879_3881dup (MSH6)	XP_024308587.1:p.Ile1293_Phe1294insLeu
XM_024452820.1:c.3696_3698dup (MSH6)	XP_024308588.1:p.Ile1232_Phe1233insLeu
XM_024452821.1:c.3582_3584dup (MSH6)	XP_024308589.1:p.Ile1194_Phe1195insLeu
XM_024452822.1:c.2973_2975dup (MSH6)	XP_024308590.1:p.Ile991_Phe992insLeu
NM_000179.3:c.3802-16_3802-14dup (MSH6) MANE Select	NP_000170.1:n.3802-16_3802-14dup
NM_001281492.2:c.3412-16_3412-14dup (MSH6)	NP_001268421.1:n.3412-16_3412-14dup
NM_001281493.2:c.2896-16_2896-14dup (MSH6)	NP_001268422.1:n.2896-16_2896-14dup
NM_001281494.2:c.2896-16_2896-14dup (MSH6)	NP_001268423.1:n.2896-16_2896-14dup