Canonical Allele Identifier: CA2580067554

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 2134359
• ClinVar RCV Id: RCV003058100 ; RCV004070118
• gnomAD v4: 2-47806651-G-GGTAACTAACTAACTATAATGGAATT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806652_47806676dup , CM000664.2:g.47806652_47806676dup	GRCh38
NC_000002.11:g.48033791_48033815dup , CM000664.1:g.48033791_48033815dup	GRCh37
NC_000002.10:g.47887295_47887319dup	NCBI36
NG_007111.1:g.28506_28530dup , LRG_219:g.28506_28530dup
NG_008397.1:g.104000_104024dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3704+1_3704+25dup (MSH6)	ENSP00000406248.2:n.3704+1_3704+25dup
ENST00000420813.6:c.3704+1_3704+25dup (MSH6)	ENSP00000390382.2:n.3704+1_3704+25dup
ENST00000455383.6:c.3704+1_3704+25dup (MSH6)	ENSP00000397484.2:n.3704+1_3704+25dup
ENST00000700004.2:c.3617+1_3617+25dup (MSH6)	ENSP00000514752.2:n.3617+1_3617+25dup
ENST00000699999.1:n.4675+1_4675+25dup (MSH6)
ENST00000700000.1:c.2435+1_2435+25dup (MSH6)	ENSP00000514749.1:n.2435+1_2435+25dup
ENST00000700002.1:c.4007+1_4007+25dup (MSH6)	ENSP00000514750.1:n.4007+1_4007+25dup
ENST00000700003.1:c.1456+1_1456+25dup (MSH6)	ENSP00000514751.1:n.1456+1_1456+25dup
ENST00000700004.1:c.2774+1_2774+25dup (MSH6)	ENSP00000514752.1:n.2774+1_2774+25dup
ENST00000700005.1:n.2853_2877dup (MSH6)
ENST00000700006.1:n.5160_5184dup (MSH6)
ENST00000700007.1:n.2596+1_2596+25dup (MSH6)
ENST00000700008.1:n.2263+1_2263+25dup (MSH6)
ENST00000700009.1:n.2665+1_2665+25dup (MSH6)
ENST00000700010.1:n.1410+1_1410+25dup (MSH6)
ENST00000700011.1:n.3295+1_3295+25dup (MSH6)
ENST00000682451.1:n.4072_4096dup (FBXO11)
ENST00000684712.1:n.4334_4358dup (FBXO11)
ENST00000234420.11:c.4001+1_4001+25dup (MSH6) MANE Select	ENSP00000234420.5:n.4001+1_4001+25dup
ENST00000540021.6:c.3611+1_3611+25dup (MSH6)	ENSP00000446475.1:n.3611+1_3611+25dup
ENST00000652107.1:c.3704+1_3704+25dup (MSH6)	ENSP00000498629.1:n.3704+1_3704+25dup
ENST00000673637.1:c.3704+1_3704+25dup (MSH6)	ENSP00000501310.1:n.3704+1_3704+25dup
ENST00000234420.9:c.4001+1_4001+25dup (MSH6)	ENSP00000234420.4:n.4001+1_4001+25dup
ENST00000405808.5:c.169+1519_169+1543dup (FBXO11)	ENSP00000385127.1:n.169+1519_169+1543dup
ENST00000434234.5:c.*124+1318_*124+1342dup (FBXO11)	ENSP00000402692.1:n.*124+1318_*124+1342dup
ENST00000445503.5:c.*3348+1_*3348+25dup (MSH6)	ENSP00000405294.1:n.*3348+1_*3348+25dup
ENST00000538136.1:c.3095+1_3095+25dup (MSH6)	ENSP00000438580.1:n.3095+1_3095+25dup
ENST00000540021.5:c.3611+1_3611+25dup (MSH6)	ENSP00000446475.1:n.3611+1_3611+25dup
ENST00000614496.4:c.3095+1_3095+25dup (MSH6)	ENSP00000477844.1:n.3095+1_3095+25dup
ENST00000622629.4:c.902+1_902+25dup (MSH6)	ENSP00000482078.1:n.902+1_902+25dup
NM_000179.2:c.4001+1_4001+25dup , LRG_219t1:c.4001+1_4001+25dup (MSH6)	NP_000170.1:n.4001+1_4001+25dup
NM_001281492.1:c.3611+1_3611+25dup (MSH6)	NP_001268421.1:n.3611+1_3611+25dup
NM_001281493.1:c.3095+1_3095+25dup (MSH6)	NP_001268422.1:n.3095+1_3095+25dup
NM_001281494.1:c.3095+1_3095+25dup (MSH6)	NP_001268423.1:n.3095+1_3095+25dup
XM_005264271.1:c.3704+1_3704+25dup (MSH6)	XP_005264328.1:n.3704+1_3704+25dup
XM_011532798.1:c.3818+1_3818+25dup (MSH6)	XP_011531100.1:n.3818+1_3818+25dup
XM_011532799.1:c.3704+1_3704+25dup (MSH6)	XP_011531101.1:n.3704+1_3704+25dup
XM_011532800.1:c.3704+1_3704+25dup (MSH6)	XP_011531102.1:n.3704+1_3704+25dup
XM_024452819.1:c.4094+1_4094+25dup (MSH6)	XP_024308587.1:n.4094+1_4094+25dup
XM_024452820.1:c.3911+1_3911+25dup (MSH6)	XP_024308588.1:n.3911+1_3911+25dup
XM_024452821.1:c.3797+1_3797+25dup (MSH6)	XP_024308589.1:n.3797+1_3797+25dup
XM_024452822.1:c.3188+1_3188+25dup (MSH6)	XP_024308590.1:n.3188+1_3188+25dup
NM_000179.3:c.4001+1_4001+25dup (MSH6) MANE Select	NP_000170.1:n.4001+1_4001+25dup
NM_001281492.2:c.3611+1_3611+25dup (MSH6)	NP_001268421.1:n.3611+1_3611+25dup
NM_001281493.2:c.3095+1_3095+25dup (MSH6)	NP_001268422.1:n.3095+1_3095+25dup
NM_001281494.2:c.3095+1_3095+25dup (MSH6)	NP_001268423.1:n.3095+1_3095+25dup