Canonical Allele Identifier: CA2658969256

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806715-G-GGGGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806720_47806724dup , CM000664.2:g.47806720_47806724dup	GRCh38
NC_000002.11:g.48033859_48033863dup , CM000664.1:g.48033859_48033863dup	GRCh37
NC_000002.10:g.47887363_47887367dup	NCBI36
NG_007111.1:g.28574_28578dup , LRG_219:g.28574_28578dup
NG_008397.1:g.103956_103960dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3705-59_3705-55dup (MSH6)	ENSP00000406248.2:n.3705-59_3705-55dup
ENST00000420813.6:c.3705-59_3705-55dup (MSH6)	ENSP00000390382.2:n.3705-59_3705-55dup
ENST00000455383.6:c.3705-59_3705-55dup (MSH6)	ENSP00000397484.2:n.3705-59_3705-55dup
ENST00000700004.2:c.3618-59_3618-55dup (MSH6)	ENSP00000514752.2:n.3618-59_3618-55dup
ENST00000699999.1:n.4676-59_4676-55dup (MSH6)
ENST00000700000.1:c.2436-59_2436-55dup (MSH6)	ENSP00000514749.1:n.2436-59_2436-55dup
ENST00000700002.1:c.4008-59_4008-55dup (MSH6)	ENSP00000514750.1:n.4008-59_4008-55dup
ENST00000700003.1:c.1457-59_1457-55dup (MSH6)	ENSP00000514751.1:n.1457-59_1457-55dup
ENST00000700004.1:c.2775-59_2775-55dup (MSH6)	ENSP00000514752.1:n.2775-59_2775-55dup
ENST00000700005.1:n.2921_2925dup (MSH6)
ENST00000700007.1:n.2597-59_2597-55dup (MSH6)
ENST00000700008.1:n.2264-59_2264-55dup (MSH6)
ENST00000700009.1:n.2666-59_2666-55dup (MSH6)
ENST00000700010.1:n.1411-59_1411-55dup (MSH6)
ENST00000700011.1:n.3296-59_3296-55dup (MSH6)
ENST00000682451.1:n.4028_4032dup (FBXO11)
ENST00000684712.1:n.4290_4294dup (FBXO11)
ENST00000234420.11:c.4002-59_4002-55dup (MSH6) MANE Select	ENSP00000234420.5:n.4002-59_4002-55dup
ENST00000540021.6:c.3612-59_3612-55dup (MSH6)	ENSP00000446475.1:n.3612-59_3612-55dup
ENST00000652107.1:c.3705-59_3705-55dup (MSH6)	ENSP00000498629.1:n.3705-59_3705-55dup
ENST00000673637.1:c.3705-59_3705-55dup (MSH6)	ENSP00000501310.1:n.3705-59_3705-55dup
ENST00000234420.9:c.4002-59_4002-55dup (MSH6)	ENSP00000234420.4:n.4002-59_4002-55dup
ENST00000405808.5:c.169+1475_169+1479dup (FBXO11)	ENSP00000385127.1:n.169+1475_169+1479dup
ENST00000434234.5:c.*124+1274_*124+1278dup (FBXO11)	ENSP00000402692.1:n.*124+1274_*124+1278dup
ENST00000445503.5:c.*3349-59_*3349-55dup (MSH6)	ENSP00000405294.1:n.*3349-59_*3349-55dup
ENST00000538136.1:c.3096-59_3096-55dup (MSH6)	ENSP00000438580.1:n.3096-59_3096-55dup
ENST00000540021.5:c.3612-59_3612-55dup (MSH6)	ENSP00000446475.1:n.3612-59_3612-55dup
ENST00000614496.4:c.3096-59_3096-55dup (MSH6)	ENSP00000477844.1:n.3096-59_3096-55dup
ENST00000622629.4:c.903-59_903-55dup (MSH6)	ENSP00000482078.1:n.903-59_903-55dup
NM_000179.2:c.4002-59_4002-55dup , LRG_219t1:c.4002-59_4002-55dup (MSH6)	NP_000170.1:n.4002-59_4002-55dup
NM_001281492.1:c.3612-59_3612-55dup (MSH6)	NP_001268421.1:n.3612-59_3612-55dup
NM_001281493.1:c.3096-59_3096-55dup (MSH6)	NP_001268422.1:n.3096-59_3096-55dup
NM_001281494.1:c.3096-59_3096-55dup (MSH6)	NP_001268423.1:n.3096-59_3096-55dup
XM_005264271.1:c.3705-59_3705-55dup (MSH6)	XP_005264328.1:n.3705-59_3705-55dup
XM_011532798.1:c.3819-59_3819-55dup (MSH6)	XP_011531100.1:n.3819-59_3819-55dup
XM_011532799.1:c.3705-59_3705-55dup (MSH6)	XP_011531101.1:n.3705-59_3705-55dup
XM_011532800.1:c.3705-59_3705-55dup (MSH6)	XP_011531102.1:n.3705-59_3705-55dup
XM_024452819.1:c.4095-59_4095-55dup (MSH6)	XP_024308587.1:n.4095-59_4095-55dup
XM_024452820.1:c.3912-59_3912-55dup (MSH6)	XP_024308588.1:n.3912-59_3912-55dup
XM_024452821.1:c.3798-59_3798-55dup (MSH6)	XP_024308589.1:n.3798-59_3798-55dup
XM_024452822.1:c.3189-59_3189-55dup (MSH6)	XP_024308590.1:n.3189-59_3189-55dup
NM_000179.3:c.4002-59_4002-55dup (MSH6) MANE Select	NP_000170.1:n.4002-59_4002-55dup
NM_001281492.2:c.3612-59_3612-55dup (MSH6)	NP_001268421.1:n.3612-59_3612-55dup
NM_001281493.2:c.3096-59_3096-55dup (MSH6)	NP_001268422.1:n.3096-59_3096-55dup
NM_001281494.2:c.3096-59_3096-55dup (MSH6)	NP_001268423.1:n.3096-59_3096-55dup