Canonical Allele Identifier: CA2658969209

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806707-C-CAGTAAAAGGGGAAGGGATGATGCACTATGAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806709_47806741dup , CM000664.2:g.47806709_47806741dup	GRCh38
NC_000002.11:g.48033848_48033880dup , CM000664.1:g.48033848_48033880dup	GRCh37
NC_000002.10:g.47887352_47887384dup	NCBI36
NG_007111.1:g.28563_28595dup , LRG_219:g.28563_28595dup
NG_008397.1:g.103936_103968dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3704+58_3705-38dup (MSH6)	ENSP00000406248.2:n.3704+58_3705-38dup
ENST00000420813.6:c.3704+58_3705-38dup (MSH6)	ENSP00000390382.2:n.3704+58_3705-38dup
ENST00000455383.6:c.3704+58_3705-38dup (MSH6)	ENSP00000397484.2:n.3704+58_3705-38dup
ENST00000700004.2:c.3617+58_3618-38dup (MSH6)	ENSP00000514752.2:n.3617+58_3618-38dup
ENST00000699999.1:n.4675+58_4676-38dup (MSH6)
ENST00000700000.1:c.2435+58_2436-38dup (MSH6)	ENSP00000514749.1:n.2435+58_2436-38dup
ENST00000700002.1:c.4007+58_4008-38dup (MSH6)	ENSP00000514750.1:n.4007+58_4008-38dup
ENST00000700003.1:c.1456+58_1457-38dup (MSH6)	ENSP00000514751.1:n.1456+58_1457-38dup
ENST00000700004.1:c.2774+58_2775-38dup (MSH6)	ENSP00000514752.1:n.2774+58_2775-38dup
ENST00000700005.1:n.2910_2942dup (MSH6)
ENST00000700007.1:n.2596+58_2597-38dup (MSH6)
ENST00000700008.1:n.2263+58_2264-38dup (MSH6)
ENST00000700009.1:n.2665+58_2666-38dup (MSH6)
ENST00000700010.1:n.1410+58_1411-38dup (MSH6)
ENST00000700011.1:n.3295+58_3296-38dup (MSH6)
ENST00000682451.1:n.4008_4040dup (FBXO11)
ENST00000684712.1:n.4270_4302dup (FBXO11)
ENST00000234420.11:c.4001+58_4002-38dup (MSH6) MANE Select	ENSP00000234420.5:n.4001+58_4002-38dup
ENST00000540021.6:c.3611+58_3612-38dup (MSH6)	ENSP00000446475.1:n.3611+58_3612-38dup
ENST00000652107.1:c.3704+58_3705-38dup (MSH6)	ENSP00000498629.1:n.3704+58_3705-38dup
ENST00000673637.1:c.3704+58_3705-38dup (MSH6)	ENSP00000501310.1:n.3704+58_3705-38dup
ENST00000234420.9:c.4001+58_4002-38dup (MSH6)	ENSP00000234420.4:n.4001+58_4002-38dup
ENST00000405808.5:c.169+1455_169+1487dup (FBXO11)	ENSP00000385127.1:n.169+1455_169+1487dup
ENST00000434234.5:c.*124+1254_*124+1286dup (FBXO11)	ENSP00000402692.1:n.*124+1254_*124+1286dup
ENST00000445503.5:c.*3348+58_*3349-38dup (MSH6)	ENSP00000405294.1:n.*3348+58_*3349-38dup
ENST00000538136.1:c.3095+58_3096-38dup (MSH6)	ENSP00000438580.1:n.3095+58_3096-38dup
ENST00000540021.5:c.3611+58_3612-38dup (MSH6)	ENSP00000446475.1:n.3611+58_3612-38dup
ENST00000614496.4:c.3095+58_3096-38dup (MSH6)	ENSP00000477844.1:n.3095+58_3096-38dup
ENST00000622629.4:c.902+58_903-38dup (MSH6)	ENSP00000482078.1:n.902+58_903-38dup
NM_000179.2:c.4001+58_4002-38dup , LRG_219t1:c.4001+58_4002-38dup (MSH6)	NP_000170.1:n.4001+58_4002-38dup
NM_001281492.1:c.3611+58_3612-38dup (MSH6)	NP_001268421.1:n.3611+58_3612-38dup
NM_001281493.1:c.3095+58_3096-38dup (MSH6)	NP_001268422.1:n.3095+58_3096-38dup
NM_001281494.1:c.3095+58_3096-38dup (MSH6)	NP_001268423.1:n.3095+58_3096-38dup
XM_005264271.1:c.3704+58_3705-38dup (MSH6)	XP_005264328.1:n.3704+58_3705-38dup
XM_011532798.1:c.3818+58_3819-38dup (MSH6)	XP_011531100.1:n.3818+58_3819-38dup
XM_011532799.1:c.3704+58_3705-38dup (MSH6)	XP_011531101.1:n.3704+58_3705-38dup
XM_011532800.1:c.3704+58_3705-38dup (MSH6)	XP_011531102.1:n.3704+58_3705-38dup
XM_024452819.1:c.4094+58_4095-38dup (MSH6)	XP_024308587.1:n.4094+58_4095-38dup
XM_024452820.1:c.3911+58_3912-38dup (MSH6)	XP_024308588.1:n.3911+58_3912-38dup
XM_024452821.1:c.3797+58_3798-38dup (MSH6)	XP_024308589.1:n.3797+58_3798-38dup
XM_024452822.1:c.3188+58_3189-38dup (MSH6)	XP_024308590.1:n.3188+58_3189-38dup
NM_000179.3:c.4001+58_4002-38dup (MSH6) MANE Select	NP_000170.1:n.4001+58_4002-38dup
NM_001281492.2:c.3611+58_3612-38dup (MSH6)	NP_001268421.1:n.3611+58_3612-38dup
NM_001281493.2:c.3095+58_3096-38dup (MSH6)	NP_001268422.1:n.3095+58_3096-38dup
NM_001281494.2:c.3095+58_3096-38dup (MSH6)	NP_001268423.1:n.3095+58_3096-38dup