Canonical Allele Identifier: CA2658967454

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806146-TTCCTTTTTTGTTTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806147_47806161del , CM000664.2:g.47806147_47806161del	GRCh38
NC_000002.11:g.48033286_48033300del , CM000664.1:g.48033286_48033300del	GRCh37
NC_000002.10:g.47886790_47886804del	NCBI36
NG_007111.1:g.28001_28015del , LRG_219:g.28001_28015del
NG_008397.1:g.104515_104529del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3350-57_3350-43del (MSH6)	ENSP00000406248.2:n.3350-57_3350-43del
ENST00000420813.6:c.3350-57_3350-43del (MSH6)	ENSP00000390382.2:n.3350-57_3350-43del
ENST00000455383.6:c.3350-57_3350-43del (MSH6)	ENSP00000397484.2:n.3350-57_3350-43del
ENST00000700004.2:c.3263-57_3263-43del (MSH6)	ENSP00000514752.2:n.3263-57_3263-43del
ENST00000699999.1:n.4321-57_4321-43del (MSH6)
ENST00000700000.1:c.2081-57_2081-43del (MSH6)	ENSP00000514749.1:n.2081-57_2081-43del
ENST00000700002.1:c.3653-57_3653-43del (MSH6)	ENSP00000514750.1:n.3653-57_3653-43del
ENST00000700003.1:c.1102-57_1102-43del (MSH6)	ENSP00000514751.1:n.1102-57_1102-43del
ENST00000700004.1:c.2420-57_2420-43del (MSH6)	ENSP00000514752.1:n.2420-57_2420-43del
ENST00000700005.1:n.2498-57_2498-43del (MSH6)
ENST00000700006.1:n.4748_4762del (MSH6)
ENST00000700007.1:n.2242-57_2242-43del (MSH6)
ENST00000700008.1:n.1816-57_1816-43del (MSH6)
ENST00000700009.1:n.2254_2268del (MSH6)
ENST00000700010.1:n.1056-57_1056-43del (MSH6)
ENST00000700011.1:n.2941-57_2941-43del (MSH6)
ENST00000682451.1:n.4587_4601del (FBXO11)
ENST00000684712.1:n.4849_4863del (FBXO11)
ENST00000234420.11:c.3647-57_3647-43del (MSH6) MANE Select	ENSP00000234420.5:n.3647-57_3647-43del
ENST00000540021.6:c.3257-57_3257-43del (MSH6)	ENSP00000446475.1:n.3257-57_3257-43del
ENST00000652107.1:c.3350-57_3350-43del (MSH6)	ENSP00000498629.1:n.3350-57_3350-43del
ENST00000673637.1:c.3350-57_3350-43del (MSH6)	ENSP00000501310.1:n.3350-57_3350-43del
ENST00000234420.9:c.3647-57_3647-43del (MSH6)	ENSP00000234420.4:n.3647-57_3647-43del
ENST00000405808.5:c.169+2034_169+2048del (FBXO11)	ENSP00000385127.1:n.169+2034_169+2048del
ENST00000434234.5:c.*124+1833_*124+1847del (FBXO11)	ENSP00000402692.1:n.*124+1833_*124+1847de...
ENST00000445503.5:c.*2994-57_*2994-43del (MSH6)	ENSP00000405294.1:n.*2994-57_*2994-43del
ENST00000538136.1:c.2741-57_2741-43del (MSH6)	ENSP00000438580.1:n.2741-57_2741-43del
ENST00000540021.5:c.3257-57_3257-43del (MSH6)	ENSP00000446475.1:n.3257-57_3257-43del
ENST00000614496.4:c.2741-57_2741-43del (MSH6)	ENSP00000477844.1:n.2741-57_2741-43del
ENST00000622629.4:c.551-57_551-43del (MSH6)	ENSP00000482078.1:n.551-57_551-43del
NM_000179.2:c.3647-57_3647-43del , LRG_219t1:c.3647-57_3647-43del (MSH6)	NP_000170.1:n.3647-57_3647-43del
NM_001281492.1:c.3257-57_3257-43del (MSH6)	NP_001268421.1:n.3257-57_3257-43del
NM_001281493.1:c.2741-57_2741-43del (MSH6)	NP_001268422.1:n.2741-57_2741-43del
NM_001281494.1:c.2741-57_2741-43del (MSH6)	NP_001268423.1:n.2741-57_2741-43del
XM_005264271.1:c.3350-57_3350-43del (MSH6)	XP_005264328.1:n.3350-57_3350-43del
XM_011532798.1:c.3464-57_3464-43del (MSH6)	XP_011531100.1:n.3464-57_3464-43del
XM_011532799.1:c.3350-57_3350-43del (MSH6)	XP_011531101.1:n.3350-57_3350-43del
XM_011532800.1:c.3350-57_3350-43del (MSH6)	XP_011531102.1:n.3350-57_3350-43del
XM_024452819.1:c.3647-57_3647-43del (MSH6)	XP_024308587.1:n.3647-57_3647-43del
XM_024452820.1:c.3464-57_3464-43del (MSH6)	XP_024308588.1:n.3464-57_3464-43del
XM_024452821.1:c.3350-57_3350-43del (MSH6)	XP_024308589.1:n.3350-57_3350-43del
XM_024452822.1:c.2741-57_2741-43del (MSH6)	XP_024308590.1:n.2741-57_2741-43del
NM_000179.3:c.3647-57_3647-43del (MSH6) MANE Select	NP_000170.1:n.3647-57_3647-43del
NM_001281492.2:c.3257-57_3257-43del (MSH6)	NP_001268421.1:n.3257-57_3257-43del
NM_001281493.2:c.2741-57_2741-43del (MSH6)	NP_001268422.1:n.2741-57_2741-43del
NM_001281494.2:c.2741-57_2741-43del (MSH6)	NP_001268423.1:n.2741-57_2741-43del