Canonical Allele Identifier: CA1030297366

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1670176112
• gnomAD v3: 2-47806707-C-CAGTAAAAGGGGAAGGGATGA
• gnomAD v4: 2-47806707-C-CAGTAAAAGGGGAAGGGATGA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806708_47806727dup , CM000664.2:g.47806708_47806727dup	GRCh38
NC_000002.11:g.48033847_48033866dup , CM000664.1:g.48033847_48033866dup	GRCh37
NC_000002.10:g.47887351_47887370dup	NCBI36
NG_007111.1:g.28562_28581dup , LRG_219:g.28562_28581dup
NG_008397.1:g.103949_103968dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3704+57_3705-52dup (MSH6)	ENSP00000406248.2:n.3704+57_3705-52dup
ENST00000420813.6:c.3704+57_3705-52dup (MSH6)	ENSP00000390382.2:n.3704+57_3705-52dup
ENST00000455383.6:c.3704+57_3705-52dup (MSH6)	ENSP00000397484.2:n.3704+57_3705-52dup
ENST00000700004.2:c.3617+57_3618-52dup (MSH6)	ENSP00000514752.2:n.3617+57_3618-52dup
ENST00000699999.1:n.4675+57_4676-52dup (MSH6)
ENST00000700000.1:c.2435+57_2436-52dup (MSH6)	ENSP00000514749.1:n.2435+57_2436-52dup
ENST00000700002.1:c.4007+57_4008-52dup (MSH6)	ENSP00000514750.1:n.4007+57_4008-52dup
ENST00000700003.1:c.1456+57_1457-52dup (MSH6)	ENSP00000514751.1:n.1456+57_1457-52dup
ENST00000700004.1:c.2774+57_2775-52dup (MSH6)	ENSP00000514752.1:n.2774+57_2775-52dup
ENST00000700005.1:n.2909_2928dup (MSH6)
ENST00000700007.1:n.2596+57_2597-52dup (MSH6)
ENST00000700008.1:n.2263+57_2264-52dup (MSH6)
ENST00000700009.1:n.2665+57_2666-52dup (MSH6)
ENST00000700010.1:n.1410+57_1411-52dup (MSH6)
ENST00000700011.1:n.3295+57_3296-52dup (MSH6)
ENST00000682451.1:n.4021_4040dup (FBXO11)
ENST00000684712.1:n.4283_4302dup (FBXO11)
ENST00000234420.11:c.4001+57_4002-52dup (MSH6) MANE Select	ENSP00000234420.5:n.4001+57_4002-52dup
ENST00000540021.6:c.3611+57_3612-52dup (MSH6)	ENSP00000446475.1:n.3611+57_3612-52dup
ENST00000652107.1:c.3704+57_3705-52dup (MSH6)	ENSP00000498629.1:n.3704+57_3705-52dup
ENST00000673637.1:c.3704+57_3705-52dup (MSH6)	ENSP00000501310.1:n.3704+57_3705-52dup
ENST00000234420.9:c.4001+57_4002-52dup (MSH6)	ENSP00000234420.4:n.4001+57_4002-52dup
ENST00000405808.5:c.169+1468_169+1487dup (FBXO11)	ENSP00000385127.1:n.169+1468_169+1487dup
ENST00000434234.5:c.*124+1267_*124+1286dup (FBXO11)	ENSP00000402692.1:n.*124+1267_*124+1286dup
ENST00000445503.5:c.*3348+57_*3349-52dup (MSH6)	ENSP00000405294.1:n.*3348+57_*3349-52dup
ENST00000538136.1:c.3095+57_3096-52dup (MSH6)	ENSP00000438580.1:n.3095+57_3096-52dup
ENST00000540021.5:c.3611+57_3612-52dup (MSH6)	ENSP00000446475.1:n.3611+57_3612-52dup
ENST00000614496.4:c.3095+57_3096-52dup (MSH6)	ENSP00000477844.1:n.3095+57_3096-52dup
ENST00000622629.4:c.902+57_903-52dup (MSH6)	ENSP00000482078.1:n.902+57_903-52dup
NM_000179.2:c.4001+57_4002-52dup , LRG_219t1:c.4001+57_4002-52dup (MSH6)	NP_000170.1:n.4001+57_4002-52dup
NM_001281492.1:c.3611+57_3612-52dup (MSH6)	NP_001268421.1:n.3611+57_3612-52dup
NM_001281493.1:c.3095+57_3096-52dup (MSH6)	NP_001268422.1:n.3095+57_3096-52dup
NM_001281494.1:c.3095+57_3096-52dup (MSH6)	NP_001268423.1:n.3095+57_3096-52dup
XM_005264271.1:c.3704+57_3705-52dup (MSH6)	XP_005264328.1:n.3704+57_3705-52dup
XM_011532798.1:c.3818+57_3819-52dup (MSH6)	XP_011531100.1:n.3818+57_3819-52dup
XM_011532799.1:c.3704+57_3705-52dup (MSH6)	XP_011531101.1:n.3704+57_3705-52dup
XM_011532800.1:c.3704+57_3705-52dup (MSH6)	XP_011531102.1:n.3704+57_3705-52dup
XM_024452819.1:c.4094+57_4095-52dup (MSH6)	XP_024308587.1:n.4094+57_4095-52dup
XM_024452820.1:c.3911+57_3912-52dup (MSH6)	XP_024308588.1:n.3911+57_3912-52dup
XM_024452821.1:c.3797+57_3798-52dup (MSH6)	XP_024308589.1:n.3797+57_3798-52dup
XM_024452822.1:c.3188+57_3189-52dup (MSH6)	XP_024308590.1:n.3188+57_3189-52dup
NM_000179.3:c.4001+57_4002-52dup (MSH6) MANE Select	NP_000170.1:n.4001+57_4002-52dup
NM_001281492.2:c.3611+57_3612-52dup (MSH6)	NP_001268421.1:n.3611+57_3612-52dup
NM_001281493.2:c.3095+57_3096-52dup (MSH6)	NP_001268422.1:n.3095+57_3096-52dup
NM_001281494.2:c.3095+57_3096-52dup (MSH6)	NP_001268423.1:n.3095+57_3096-52dup