Canonical Allele Identifier: CA2576961621

Gene: MSH6 FBXO11

Linked Data

• gnomAD v3: 2-47806699-CAAAG-C
• gnomAD v4: 2-47806699-CAAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806703_47806706del , CM000664.2:g.47806703_47806706del	GRCh38
NC_000002.11:g.48033842_48033845del , CM000664.1:g.48033842_48033845del	GRCh37
NC_000002.10:g.47887346_47887349del	NCBI36
NG_007111.1:g.28557_28560del , LRG_219:g.28557_28560del
NG_008397.1:g.103973_103976del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3704+52_3704+55del (MSH6)	ENSP00000406248.2:n.3704+52_3704+55del
ENST00000420813.6:c.3704+52_3704+55del (MSH6)	ENSP00000390382.2:n.3704+52_3704+55del
ENST00000455383.6:c.3704+52_3704+55del (MSH6)	ENSP00000397484.2:n.3704+52_3704+55del
ENST00000700004.2:c.3617+52_3617+55del (MSH6)	ENSP00000514752.2:n.3617+52_3617+55del
ENST00000699999.1:n.4675+52_4675+55del (MSH6)
ENST00000700000.1:c.2435+52_2435+55del (MSH6)	ENSP00000514749.1:n.2435+52_2435+55del
ENST00000700002.1:c.4007+52_4007+55del (MSH6)	ENSP00000514750.1:n.4007+52_4007+55del
ENST00000700003.1:c.1456+52_1456+55del (MSH6)	ENSP00000514751.1:n.1456+52_1456+55del
ENST00000700004.1:c.2774+52_2774+55del (MSH6)	ENSP00000514752.1:n.2774+52_2774+55del
ENST00000700005.1:n.2904_2907del (MSH6)
ENST00000700006.1:n.5211_5214del (MSH6)
ENST00000700007.1:n.2596+52_2596+55del (MSH6)
ENST00000700008.1:n.2263+52_2263+55del (MSH6)
ENST00000700009.1:n.2665+52_2665+55del (MSH6)
ENST00000700010.1:n.1410+52_1410+55del (MSH6)
ENST00000700011.1:n.3295+52_3295+55del (MSH6)
ENST00000682451.1:n.4045_4048del (FBXO11)
ENST00000684712.1:n.4307_4310del (FBXO11)
ENST00000234420.11:c.4001+52_4001+55del (MSH6) MANE Select	ENSP00000234420.5:n.4001+52_4001+55del
ENST00000540021.6:c.3611+52_3611+55del (MSH6)	ENSP00000446475.1:n.3611+52_3611+55del
ENST00000652107.1:c.3704+52_3704+55del (MSH6)	ENSP00000498629.1:n.3704+52_3704+55del
ENST00000673637.1:c.3704+52_3704+55del (MSH6)	ENSP00000501310.1:n.3704+52_3704+55del
ENST00000234420.9:c.4001+52_4001+55del (MSH6)	ENSP00000234420.4:n.4001+52_4001+55del
ENST00000405808.5:c.169+1492_169+1495del (FBXO11)	ENSP00000385127.1:n.169+1492_169+1495del
ENST00000434234.5:c.*124+1291_*124+1294del (FBXO11)	ENSP00000402692.1:n.*124+1291_*124+1294del
ENST00000445503.5:c.*3348+52_*3348+55del (MSH6)	ENSP00000405294.1:n.*3348+52_*3348+55del
ENST00000538136.1:c.3095+52_3095+55del (MSH6)	ENSP00000438580.1:n.3095+52_3095+55del
ENST00000540021.5:c.3611+52_3611+55del (MSH6)	ENSP00000446475.1:n.3611+52_3611+55del
ENST00000614496.4:c.3095+52_3095+55del (MSH6)	ENSP00000477844.1:n.3095+52_3095+55del
ENST00000622629.4:c.902+52_902+55del (MSH6)	ENSP00000482078.1:n.902+52_902+55del
NM_000179.2:c.4001+52_4001+55del , LRG_219t1:c.4001+52_4001+55del (MSH6)	NP_000170.1:n.4001+52_4001+55del
NM_001281492.1:c.3611+52_3611+55del (MSH6)	NP_001268421.1:n.3611+52_3611+55del
NM_001281493.1:c.3095+52_3095+55del (MSH6)	NP_001268422.1:n.3095+52_3095+55del
NM_001281494.1:c.3095+52_3095+55del (MSH6)	NP_001268423.1:n.3095+52_3095+55del
XM_005264271.1:c.3704+52_3704+55del (MSH6)	XP_005264328.1:n.3704+52_3704+55del
XM_011532798.1:c.3818+52_3818+55del (MSH6)	XP_011531100.1:n.3818+52_3818+55del
XM_011532799.1:c.3704+52_3704+55del (MSH6)	XP_011531101.1:n.3704+52_3704+55del
XM_011532800.1:c.3704+52_3704+55del (MSH6)	XP_011531102.1:n.3704+52_3704+55del
XM_024452819.1:c.4094+52_4094+55del (MSH6)	XP_024308587.1:n.4094+52_4094+55del
XM_024452820.1:c.3911+52_3911+55del (MSH6)	XP_024308588.1:n.3911+52_3911+55del
XM_024452821.1:c.3797+52_3797+55del (MSH6)	XP_024308589.1:n.3797+52_3797+55del
XM_024452822.1:c.3188+52_3188+55del (MSH6)	XP_024308590.1:n.3188+52_3188+55del
NM_000179.3:c.4001+52_4001+55del (MSH6) MANE Select	NP_000170.1:n.4001+52_4001+55del
NM_001281492.2:c.3611+52_3611+55del (MSH6)	NP_001268421.1:n.3611+52_3611+55del
NM_001281493.2:c.3095+52_3095+55del (MSH6)	NP_001268422.1:n.3095+52_3095+55del
NM_001281494.2:c.3095+52_3095+55del (MSH6)	NP_001268423.1:n.3095+52_3095+55del