Canonical Allele Identifier: CA2658969485

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806743-CAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806748_47806750del , CM000664.2:g.47806748_47806750del	GRCh38
NC_000002.11:g.48033887_48033889del , CM000664.1:g.48033887_48033889del	GRCh37
NC_000002.10:g.47887391_47887393del	NCBI36
NG_007111.1:g.28602_28604del , LRG_219:g.28602_28604del
NG_008397.1:g.103930_103932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3705-31_3705-29del (MSH6)	ENSP00000406248.2:n.3705-31_3705-29del
ENST00000420813.6:c.3705-31_3705-29del (MSH6)	ENSP00000390382.2:n.3705-31_3705-29del
ENST00000455383.6:c.3705-31_3705-29del (MSH6)	ENSP00000397484.2:n.3705-31_3705-29del
ENST00000700004.2:c.3618-31_3618-29del (MSH6)	ENSP00000514752.2:n.3618-31_3618-29del
ENST00000699999.1:n.4676-31_4676-29del (MSH6)
ENST00000700000.1:c.2436-31_2436-29del (MSH6)	ENSP00000514749.1:n.2436-31_2436-29del
ENST00000700002.1:c.4008-31_4008-29del (MSH6)	ENSP00000514750.1:n.4008-31_4008-29del
ENST00000700003.1:c.1457-31_1457-29del (MSH6)	ENSP00000514751.1:n.1457-31_1457-29del
ENST00000700004.1:c.2775-31_2775-29del (MSH6)	ENSP00000514752.1:n.2775-31_2775-29del
ENST00000700005.1:n.2949_2951del (MSH6)
ENST00000700007.1:n.2597-31_2597-29del (MSH6)
ENST00000700008.1:n.2264-31_2264-29del (MSH6)
ENST00000700009.1:n.2666-31_2666-29del (MSH6)
ENST00000700010.1:n.1411-31_1411-29del (MSH6)
ENST00000700011.1:n.3296-31_3296-29del (MSH6)
ENST00000682451.1:n.4002_4004del (FBXO11)
ENST00000684712.1:n.4264_4266del (FBXO11)
ENST00000234420.11:c.4002-31_4002-29del (MSH6) MANE Select	ENSP00000234420.5:n.4002-31_4002-29del
ENST00000540021.6:c.3612-31_3612-29del (MSH6)	ENSP00000446475.1:n.3612-31_3612-29del
ENST00000652107.1:c.3705-31_3705-29del (MSH6)	ENSP00000498629.1:n.3705-31_3705-29del
ENST00000673637.1:c.3705-31_3705-29del (MSH6)	ENSP00000501310.1:n.3705-31_3705-29del
ENST00000234420.9:c.4002-31_4002-29del (MSH6)	ENSP00000234420.4:n.4002-31_4002-29del
ENST00000405808.5:c.169+1449_169+1451del (FBXO11)	ENSP00000385127.1:n.169+1449_169+1451del
ENST00000434234.5:c.*124+1248_*124+1250del (FBXO11)	ENSP00000402692.1:n.*124+1248_*124+1250del
ENST00000445503.5:c.*3349-31_*3349-29del (MSH6)	ENSP00000405294.1:n.*3349-31_*3349-29del
ENST00000538136.1:c.3096-31_3096-29del (MSH6)	ENSP00000438580.1:n.3096-31_3096-29del
ENST00000540021.5:c.3612-31_3612-29del (MSH6)	ENSP00000446475.1:n.3612-31_3612-29del
ENST00000614496.4:c.3096-31_3096-29del (MSH6)	ENSP00000477844.1:n.3096-31_3096-29del
ENST00000622629.4:c.903-31_903-29del (MSH6)	ENSP00000482078.1:n.903-31_903-29del
NM_000179.2:c.4002-31_4002-29del , LRG_219t1:c.4002-31_4002-29del (MSH6)	NP_000170.1:n.4002-31_4002-29del
NM_001281492.1:c.3612-31_3612-29del (MSH6)	NP_001268421.1:n.3612-31_3612-29del
NM_001281493.1:c.3096-31_3096-29del (MSH6)	NP_001268422.1:n.3096-31_3096-29del
NM_001281494.1:c.3096-31_3096-29del (MSH6)	NP_001268423.1:n.3096-31_3096-29del
XM_005264271.1:c.3705-31_3705-29del (MSH6)	XP_005264328.1:n.3705-31_3705-29del
XM_011532798.1:c.3819-31_3819-29del (MSH6)	XP_011531100.1:n.3819-31_3819-29del
XM_011532799.1:c.3705-31_3705-29del (MSH6)	XP_011531101.1:n.3705-31_3705-29del
XM_011532800.1:c.3705-31_3705-29del (MSH6)	XP_011531102.1:n.3705-31_3705-29del
XM_024452819.1:c.4095-31_4095-29del (MSH6)	XP_024308587.1:n.4095-31_4095-29del
XM_024452820.1:c.3912-31_3912-29del (MSH6)	XP_024308588.1:n.3912-31_3912-29del
XM_024452821.1:c.3798-31_3798-29del (MSH6)	XP_024308589.1:n.3798-31_3798-29del
XM_024452822.1:c.3189-31_3189-29del (MSH6)	XP_024308590.1:n.3189-31_3189-29del
NM_000179.3:c.4002-31_4002-29del (MSH6) MANE Select	NP_000170.1:n.4002-31_4002-29del
NM_001281492.2:c.3612-31_3612-29del (MSH6)	NP_001268421.1:n.3612-31_3612-29del
NM_001281493.2:c.3096-31_3096-29del (MSH6)	NP_001268422.1:n.3096-31_3096-29del
NM_001281494.2:c.3096-31_3096-29del (MSH6)	NP_001268423.1:n.3096-31_3096-29del