Canonical Allele Identifier: CA2658965980

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47805094-C-CTTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805095_47805098dup , CM000664.2:g.47805095_47805098dup	GRCh38
NC_000002.11:g.48032234_48032237dup , CM000664.1:g.48032234_48032237dup	GRCh37
NC_000002.10:g.47885738_47885741dup	NCBI36
NG_007111.1:g.26949_26952dup , LRG_219:g.26949_26952dup
NG_008397.1:g.105578_105581dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3259+68_3259+71dup (MSH6)	ENSP00000406248.2:n.3259+68_3259+71dup
ENST00000420813.6:c.3259+68_3259+71dup (MSH6)	ENSP00000390382.2:n.3259+68_3259+71dup
ENST00000455383.6:c.3259+68_3259+71dup (MSH6)	ENSP00000397484.2:n.3259+68_3259+71dup
ENST00000700004.2:c.3173-523_3173-520dup (MSH6)	ENSP00000514752.2:n.3173-523_3173-520dup
ENST00000699999.1:n.3708_3711dup (MSH6)
ENST00000700000.1:c.1990+68_1990+71dup (MSH6)	ENSP00000514749.1:n.1990+68_1990+71dup
ENST00000700002.1:c.3562+68_3562+71dup (MSH6)	ENSP00000514750.1:n.3562+68_3562+71dup
ENST00000700003.1:c.1011+68_1011+71dup (MSH6)	ENSP00000514751.1:n.1011+68_1011+71dup
ENST00000700004.1:c.2330-523_2330-520dup (MSH6)	ENSP00000514752.1:n.2330-523_2330-520dup
ENST00000700005.1:n.2407+68_2407+71dup (MSH6)
ENST00000700006.1:n.3696_3699dup (MSH6)
ENST00000700007.1:n.1629_1632dup (MSH6)
ENST00000700008.1:n.1203_1206dup (MSH6)
ENST00000700009.1:n.1202_1205dup (MSH6)
ENST00000700010.1:n.965+68_965+71dup (MSH6)
ENST00000700011.1:n.2328_2331dup (MSH6)
ENST00000234420.11:c.3556+68_3556+71dup (MSH6) MANE Select	ENSP00000234420.5:n.3556+68_3556+71dup
ENST00000540021.6:c.3166+68_3166+71dup (MSH6)	ENSP00000446475.1:n.3166+68_3166+71dup
ENST00000652107.1:c.3259+68_3259+71dup (MSH6)	ENSP00000498629.1:n.3259+68_3259+71dup
ENST00000673637.1:c.3259+68_3259+71dup (MSH6)	ENSP00000501310.1:n.3259+68_3259+71dup
ENST00000234420.9:c.3556+68_3556+71dup (MSH6)	ENSP00000234420.4:n.3556+68_3556+71dup
ENST00000405808.5:c.169+3097_169+3100dup (FBXO11)	ENSP00000385127.1:n.169+3097_169+3100dup
ENST00000434234.5:c.*124+2896_*124+2899dup (FBXO11)	ENSP00000402692.1:n.*124+2896_*124+2899dup
ENST00000445503.5:c.*2903+68_*2903+71dup (MSH6)	ENSP00000405294.1:n.*2903+68_*2903+71dup
ENST00000538136.1:c.2650+68_2650+71dup (MSH6)	ENSP00000438580.1:n.2650+68_2650+71dup
ENST00000540021.5:c.3166+68_3166+71dup (MSH6)	ENSP00000446475.1:n.3166+68_3166+71dup
ENST00000614496.4:c.2650+68_2650+71dup (MSH6)	ENSP00000477844.1:n.2650+68_2650+71dup
ENST00000622629.4:c.460+68_460+71dup (MSH6)	ENSP00000482078.1:n.460+68_460+71dup
NM_000179.2:c.3556+68_3556+71dup , LRG_219t1:c.3556+68_3556+71dup (MSH6)	NP_000170.1:n.3556+68_3556+71dup
NM_001281492.1:c.3166+68_3166+71dup (MSH6)	NP_001268421.1:n.3166+68_3166+71dup
NM_001281493.1:c.2650+68_2650+71dup (MSH6)	NP_001268422.1:n.2650+68_2650+71dup
NM_001281494.1:c.2650+68_2650+71dup (MSH6)	NP_001268423.1:n.2650+68_2650+71dup
XM_005264271.1:c.3259+68_3259+71dup (MSH6)	XP_005264328.1:n.3259+68_3259+71dup
XM_011532798.1:c.3373+68_3373+71dup (MSH6)	XP_011531100.1:n.3373+68_3373+71dup
XM_011532799.1:c.3259+68_3259+71dup (MSH6)	XP_011531101.1:n.3259+68_3259+71dup
XM_011532800.1:c.3259+68_3259+71dup (MSH6)	XP_011531102.1:n.3259+68_3259+71dup
XM_024452819.1:c.3556+68_3556+71dup (MSH6)	XP_024308587.1:n.3556+68_3556+71dup
XM_024452820.1:c.3373+68_3373+71dup (MSH6)	XP_024308588.1:n.3373+68_3373+71dup
XM_024452821.1:c.3259+68_3259+71dup (MSH6)	XP_024308589.1:n.3259+68_3259+71dup
XM_024452822.1:c.2650+68_2650+71dup (MSH6)	XP_024308590.1:n.2650+68_2650+71dup
NM_000179.3:c.3556+68_3556+71dup (MSH6) MANE Select	NP_000170.1:n.3556+68_3556+71dup
NM_001281492.2:c.3166+68_3166+71dup (MSH6)	NP_001268421.1:n.3166+68_3166+71dup
NM_001281493.2:c.2650+68_2650+71dup (MSH6)	NP_001268422.1:n.2650+68_2650+71dup
NM_001281494.2:c.2650+68_2650+71dup (MSH6)	NP_001268423.1:n.2650+68_2650+71dup