Canonical Allele Identifier: CA2658967980

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806411-T-TGTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806411_47806412insGTTG , CM000664.2:g.47806411_47806412insGTTG	GRCh38
NC_000002.11:g.48033550_48033551insGTTG , CM000664.1:g.48033550_48033551insGTTG	GRCh37
NC_000002.10:g.47887054_47887055insGTTG	NCBI36
NG_007111.1:g.28265_28266insGTTG , LRG_219:g.28265_28266insGTTG
NG_008397.1:g.104264_104265insCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3505-41_3505-40insGTTG (MSH6)	ENSP00000406248.2:n.3505-41_3505-40insGTTG
ENST00000420813.6:c.3505-41_3505-40insGTTG (MSH6)	ENSP00000390382.2:n.3505-41_3505-40insGTTG
ENST00000455383.6:c.3505-41_3505-40insGTTG (MSH6)	ENSP00000397484.2:n.3505-41_3505-40insGTTG
ENST00000700004.2:c.3418-41_3418-40insGTTG (MSH6)	ENSP00000514752.2:n.3418-41_3418-40insGTTG
ENST00000699999.1:n.4476-41_4476-40insGTTG (MSH6)
ENST00000700000.1:c.2236-41_2236-40insGTTG (MSH6)	ENSP00000514749.1:n.2236-41_2236-40insGTTG
ENST00000700002.1:c.3808-41_3808-40insGTTG (MSH6)	ENSP00000514750.1:n.3808-41_3808-40insGTTG
ENST00000700003.1:c.1257-41_1257-40insGTTG (MSH6)	ENSP00000514751.1:n.1257-41_1257-40insGTTG
ENST00000700004.1:c.2575-41_2575-40insGTTG (MSH6)	ENSP00000514752.1:n.2575-41_2575-40insGTTG
ENST00000700005.1:n.2653-41_2653-40insGTTG (MSH6)
ENST00000700006.1:n.4960-41_4960-40insGTTG (MSH6)
ENST00000700007.1:n.2397-41_2397-40insGTTG (MSH6)
ENST00000700008.1:n.2023_2024insGTTG (MSH6)
ENST00000700009.1:n.2466-41_2466-40insGTTG (MSH6)
ENST00000700010.1:n.1211-41_1211-40insGTTG (MSH6)
ENST00000700011.1:n.3096-41_3096-40insGTTG (MSH6)
ENST00000682451.1:n.4336_4337insCAAC (FBXO11)
ENST00000684712.1:n.4598_4599insCAAC (FBXO11)
ENST00000234420.11:c.3802-41_3802-40insGTTG (MSH6) MANE Select	ENSP00000234420.5:n.3802-41_3802-40insGTTG
ENST00000540021.6:c.3412-41_3412-40insGTTG (MSH6)	ENSP00000446475.1:n.3412-41_3412-40insGTTG
ENST00000652107.1:c.3505-41_3505-40insGTTG (MSH6)	ENSP00000498629.1:n.3505-41_3505-40insGTTG
ENST00000673637.1:c.3505-41_3505-40insGTTG (MSH6)	ENSP00000501310.1:n.3505-41_3505-40insGTTG
ENST00000234420.9:c.3802-41_3802-40insGTTG (MSH6)	ENSP00000234420.4:n.3802-41_3802-40insGTTG
ENST00000405808.5:c.169+1783_169+1784insCAAC (FBXO11)	ENSP00000385127.1:n.169+1783_169+1784insCAAC
ENST00000434234.5:c.*124+1582_*124+1583insCAAC (FBXO11)	ENSP00000402692.1:n.*124+1582_*124+1583insCAAC
ENST00000445503.5:c.*3149-41_*3149-40insGTTG (MSH6)	ENSP00000405294.1:n.*3149-41_*3149-40insGTTG
ENST00000538136.1:c.2896-41_2896-40insGTTG (MSH6)	ENSP00000438580.1:n.2896-41_2896-40insGTTG
ENST00000540021.5:c.3412-41_3412-40insGTTG (MSH6)	ENSP00000446475.1:n.3412-41_3412-40insGTTG
ENST00000614496.4:c.2896-41_2896-40insGTTG (MSH6)	ENSP00000477844.1:n.2896-41_2896-40insGTTG
ENST00000622629.4:c.703-41_703-40insGTTG (MSH6)	ENSP00000482078.1:n.703-41_703-40insGTTG
NM_000179.2:c.3802-41_3802-40insGTTG , LRG_219t1:c.3802-41_3802-40insGTTG (MSH6)	NP_000170.1:n.3802-41_3802-40insGTTG
NM_001281492.1:c.3412-41_3412-40insGTTG (MSH6)	NP_001268421.1:n.3412-41_3412-40insGTTG
NM_001281493.1:c.2896-41_2896-40insGTTG (MSH6)	NP_001268422.1:n.2896-41_2896-40insGTTG
NM_001281494.1:c.2896-41_2896-40insGTTG (MSH6)	NP_001268423.1:n.2896-41_2896-40insGTTG
XM_005264271.1:c.3505-41_3505-40insGTTG (MSH6)	XP_005264328.1:n.3505-41_3505-40insGTTG
XM_011532798.1:c.3619-41_3619-40insGTTG (MSH6)	XP_011531100.1:n.3619-41_3619-40insGTTG
XM_011532799.1:c.3505-41_3505-40insGTTG (MSH6)	XP_011531101.1:n.3505-41_3505-40insGTTG
XM_011532800.1:c.3505-41_3505-40insGTTG (MSH6)	XP_011531102.1:n.3505-41_3505-40insGTTG
XM_024452819.1:c.3854_3855insGTTG (MSH6)	XP_024308587.1:p.His1289SerfsTer11
XM_024452820.1:c.3671_3672insGTTG (MSH6)	XP_024308588.1:p.His1228SerfsTer11
XM_024452821.1:c.3557_3558insGTTG (MSH6)	XP_024308589.1:p.His1190SerfsTer11
XM_024452822.1:c.2948_2949insGTTG (MSH6)	XP_024308590.1:p.His987SerfsTer11
NM_000179.3:c.3802-41_3802-40insGTTG (MSH6) MANE Select	NP_000170.1:n.3802-41_3802-40insGTTG
NM_001281492.2:c.3412-41_3412-40insGTTG (MSH6)	NP_001268421.1:n.3412-41_3412-40insGTTG
NM_001281493.2:c.2896-41_2896-40insGTTG (MSH6)	NP_001268422.1:n.2896-41_2896-40insGTTG
NM_001281494.2:c.2896-41_2896-40insGTTG (MSH6)	NP_001268423.1:n.2896-41_2896-40insGTTG