Canonical Allele Identifier: CA2658969107

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806693-A-AAGTTTCAAAGAAACAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806695_47806711dup , CM000664.2:g.47806695_47806711dup	GRCh38
NC_000002.11:g.48033834_48033850dup , CM000664.1:g.48033834_48033850dup	GRCh37
NC_000002.10:g.47887338_47887354dup	NCBI36
NG_007111.1:g.28549_28565dup , LRG_219:g.28549_28565dup
NG_008397.1:g.103966_103982dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3704+44_3704+60dup (MSH6)	ENSP00000406248.2:n.3704+44_3704+60dup
ENST00000420813.6:c.3704+44_3704+60dup (MSH6)	ENSP00000390382.2:n.3704+44_3704+60dup
ENST00000455383.6:c.3704+44_3704+60dup (MSH6)	ENSP00000397484.2:n.3704+44_3704+60dup
ENST00000700004.2:c.3617+44_3617+60dup (MSH6)	ENSP00000514752.2:n.3617+44_3617+60dup
ENST00000699999.1:n.4675+44_4675+60dup (MSH6)
ENST00000700000.1:c.2435+44_2435+60dup (MSH6)	ENSP00000514749.1:n.2435+44_2435+60dup
ENST00000700002.1:c.4007+44_4007+60dup (MSH6)	ENSP00000514750.1:n.4007+44_4007+60dup
ENST00000700003.1:c.1456+44_1456+60dup (MSH6)	ENSP00000514751.1:n.1456+44_1456+60dup
ENST00000700004.1:c.2774+44_2774+60dup (MSH6)	ENSP00000514752.1:n.2774+44_2774+60dup
ENST00000700005.1:n.2896_2912dup (MSH6)
ENST00000700006.1:n.5203_5219dup (MSH6)
ENST00000700007.1:n.2596+44_2596+60dup (MSH6)
ENST00000700008.1:n.2263+44_2263+60dup (MSH6)
ENST00000700009.1:n.2665+44_2665+60dup (MSH6)
ENST00000700010.1:n.1410+44_1410+60dup (MSH6)
ENST00000700011.1:n.3295+44_3295+60dup (MSH6)
ENST00000682451.1:n.4038_4054dup (FBXO11)
ENST00000684712.1:n.4300_4316dup (FBXO11)
ENST00000234420.11:c.4001+44_4001+60dup (MSH6) MANE Select	ENSP00000234420.5:n.4001+44_4001+60dup
ENST00000540021.6:c.3611+44_3611+60dup (MSH6)	ENSP00000446475.1:n.3611+44_3611+60dup
ENST00000652107.1:c.3704+44_3704+60dup (MSH6)	ENSP00000498629.1:n.3704+44_3704+60dup
ENST00000673637.1:c.3704+44_3704+60dup (MSH6)	ENSP00000501310.1:n.3704+44_3704+60dup
ENST00000234420.9:c.4001+44_4001+60dup (MSH6)	ENSP00000234420.4:n.4001+44_4001+60dup
ENST00000405808.5:c.169+1485_169+1501dup (FBXO11)	ENSP00000385127.1:n.169+1485_169+1501dup
ENST00000434234.5:c.*124+1284_*124+1300dup (FBXO11)	ENSP00000402692.1:n.*124+1284_*124+1300dup
ENST00000445503.5:c.*3348+44_*3348+60dup (MSH6)	ENSP00000405294.1:n.*3348+44_*3348+60dup
ENST00000538136.1:c.3095+44_3095+60dup (MSH6)	ENSP00000438580.1:n.3095+44_3095+60dup
ENST00000540021.5:c.3611+44_3611+60dup (MSH6)	ENSP00000446475.1:n.3611+44_3611+60dup
ENST00000614496.4:c.3095+44_3095+60dup (MSH6)	ENSP00000477844.1:n.3095+44_3095+60dup
ENST00000622629.4:c.902+44_902+60dup (MSH6)	ENSP00000482078.1:n.902+44_902+60dup
NM_000179.2:c.4001+44_4001+60dup , LRG_219t1:c.4001+44_4001+60dup (MSH6)	NP_000170.1:n.4001+44_4001+60dup
NM_001281492.1:c.3611+44_3611+60dup (MSH6)	NP_001268421.1:n.3611+44_3611+60dup
NM_001281493.1:c.3095+44_3095+60dup (MSH6)	NP_001268422.1:n.3095+44_3095+60dup
NM_001281494.1:c.3095+44_3095+60dup (MSH6)	NP_001268423.1:n.3095+44_3095+60dup
XM_005264271.1:c.3704+44_3704+60dup (MSH6)	XP_005264328.1:n.3704+44_3704+60dup
XM_011532798.1:c.3818+44_3818+60dup (MSH6)	XP_011531100.1:n.3818+44_3818+60dup
XM_011532799.1:c.3704+44_3704+60dup (MSH6)	XP_011531101.1:n.3704+44_3704+60dup
XM_011532800.1:c.3704+44_3704+60dup (MSH6)	XP_011531102.1:n.3704+44_3704+60dup
XM_024452819.1:c.4094+44_4094+60dup (MSH6)	XP_024308587.1:n.4094+44_4094+60dup
XM_024452820.1:c.3911+44_3911+60dup (MSH6)	XP_024308588.1:n.3911+44_3911+60dup
XM_024452821.1:c.3797+44_3797+60dup (MSH6)	XP_024308589.1:n.3797+44_3797+60dup
XM_024452822.1:c.3188+44_3188+60dup (MSH6)	XP_024308590.1:n.3188+44_3188+60dup
NM_000179.3:c.4001+44_4001+60dup (MSH6) MANE Select	NP_000170.1:n.4001+44_4001+60dup
NM_001281492.2:c.3611+44_3611+60dup (MSH6)	NP_001268421.1:n.3611+44_3611+60dup
NM_001281493.2:c.3095+44_3095+60dup (MSH6)	NP_001268422.1:n.3095+44_3095+60dup
NM_001281494.2:c.3095+44_3095+60dup (MSH6)	NP_001268423.1:n.3095+44_3095+60dup