Canonical Allele Identifier: CA2658968993

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806678-T-TAACTA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806680_47806684dup , CM000664.2:g.47806680_47806684dup	GRCh38
NC_000002.11:g.48033819_48033823dup , CM000664.1:g.48033819_48033823dup	GRCh37
NC_000002.10:g.47887323_47887327dup	NCBI36
NG_007111.1:g.28534_28538dup , LRG_219:g.28534_28538dup
NG_008397.1:g.103993_103997dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3704+29_3704+33dup (MSH6)	ENSP00000406248.2:n.3704+29_3704+33dup
ENST00000420813.6:c.3704+29_3704+33dup (MSH6)	ENSP00000390382.2:n.3704+29_3704+33dup
ENST00000455383.6:c.3704+29_3704+33dup (MSH6)	ENSP00000397484.2:n.3704+29_3704+33dup
ENST00000700004.2:c.3617+29_3617+33dup (MSH6)	ENSP00000514752.2:n.3617+29_3617+33dup
ENST00000699999.1:n.4675+29_4675+33dup (MSH6)
ENST00000700000.1:c.2435+29_2435+33dup (MSH6)	ENSP00000514749.1:n.2435+29_2435+33dup
ENST00000700002.1:c.4007+29_4007+33dup (MSH6)	ENSP00000514750.1:n.4007+29_4007+33dup
ENST00000700003.1:c.1456+29_1456+33dup (MSH6)	ENSP00000514751.1:n.1456+29_1456+33dup
ENST00000700004.1:c.2774+29_2774+33dup (MSH6)	ENSP00000514752.1:n.2774+29_2774+33dup
ENST00000700005.1:n.2881_2885dup (MSH6)
ENST00000700006.1:n.5188_5192dup (MSH6)
ENST00000700007.1:n.2596+29_2596+33dup (MSH6)
ENST00000700008.1:n.2263+29_2263+33dup (MSH6)
ENST00000700009.1:n.2665+29_2665+33dup (MSH6)
ENST00000700010.1:n.1410+29_1410+33dup (MSH6)
ENST00000700011.1:n.3295+29_3295+33dup (MSH6)
ENST00000682451.1:n.4065_4069dup (FBXO11)
ENST00000684712.1:n.4327_4331dup (FBXO11)
ENST00000234420.11:c.4001+29_4001+33dup (MSH6) MANE Select	ENSP00000234420.5:n.4001+29_4001+33dup
ENST00000540021.6:c.3611+29_3611+33dup (MSH6)	ENSP00000446475.1:n.3611+29_3611+33dup
ENST00000652107.1:c.3704+29_3704+33dup (MSH6)	ENSP00000498629.1:n.3704+29_3704+33dup
ENST00000673637.1:c.3704+29_3704+33dup (MSH6)	ENSP00000501310.1:n.3704+29_3704+33dup
ENST00000234420.9:c.4001+29_4001+33dup (MSH6)	ENSP00000234420.4:n.4001+29_4001+33dup
ENST00000405808.5:c.169+1512_169+1516dup (FBXO11)	ENSP00000385127.1:n.169+1512_169+1516dup
ENST00000434234.5:c.*124+1311_*124+1315dup (FBXO11)	ENSP00000402692.1:n.*124+1311_*124+1315dup
ENST00000445503.5:c.*3348+29_*3348+33dup (MSH6)	ENSP00000405294.1:n.*3348+29_*3348+33dup
ENST00000538136.1:c.3095+29_3095+33dup (MSH6)	ENSP00000438580.1:n.3095+29_3095+33dup
ENST00000540021.5:c.3611+29_3611+33dup (MSH6)	ENSP00000446475.1:n.3611+29_3611+33dup
ENST00000614496.4:c.3095+29_3095+33dup (MSH6)	ENSP00000477844.1:n.3095+29_3095+33dup
ENST00000622629.4:c.902+29_902+33dup (MSH6)	ENSP00000482078.1:n.902+29_902+33dup
NM_000179.2:c.4001+29_4001+33dup , LRG_219t1:c.4001+29_4001+33dup (MSH6)	NP_000170.1:n.4001+29_4001+33dup
NM_001281492.1:c.3611+29_3611+33dup (MSH6)	NP_001268421.1:n.3611+29_3611+33dup
NM_001281493.1:c.3095+29_3095+33dup (MSH6)	NP_001268422.1:n.3095+29_3095+33dup
NM_001281494.1:c.3095+29_3095+33dup (MSH6)	NP_001268423.1:n.3095+29_3095+33dup
XM_005264271.1:c.3704+29_3704+33dup (MSH6)	XP_005264328.1:n.3704+29_3704+33dup
XM_011532798.1:c.3818+29_3818+33dup (MSH6)	XP_011531100.1:n.3818+29_3818+33dup
XM_011532799.1:c.3704+29_3704+33dup (MSH6)	XP_011531101.1:n.3704+29_3704+33dup
XM_011532800.1:c.3704+29_3704+33dup (MSH6)	XP_011531102.1:n.3704+29_3704+33dup
XM_024452819.1:c.4094+29_4094+33dup (MSH6)	XP_024308587.1:n.4094+29_4094+33dup
XM_024452820.1:c.3911+29_3911+33dup (MSH6)	XP_024308588.1:n.3911+29_3911+33dup
XM_024452821.1:c.3797+29_3797+33dup (MSH6)	XP_024308589.1:n.3797+29_3797+33dup
XM_024452822.1:c.3188+29_3188+33dup (MSH6)	XP_024308590.1:n.3188+29_3188+33dup
NM_000179.3:c.4001+29_4001+33dup (MSH6) MANE Select	NP_000170.1:n.4001+29_4001+33dup
NM_001281492.2:c.3611+29_3611+33dup (MSH6)	NP_001268421.1:n.3611+29_3611+33dup
NM_001281493.2:c.3095+29_3095+33dup (MSH6)	NP_001268422.1:n.3095+29_3095+33dup
NM_001281494.2:c.3095+29_3095+33dup (MSH6)	NP_001268423.1:n.3095+29_3095+33dup