Canonical Allele Identifier: CA2658967447

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806139-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806142_47806143dup , CM000664.2:g.47806142_47806143dup	GRCh38
NC_000002.11:g.48033281_48033282dup , CM000664.1:g.48033281_48033282dup	GRCh37
NC_000002.10:g.47886785_47886786dup	NCBI36
NG_007111.1:g.27996_27997dup , LRG_219:g.27996_27997dup
NG_008397.1:g.104535_104536dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3350-62_3350-61dup (MSH6)	ENSP00000406248.2:n.3350-62_3350-61dup
ENST00000420813.6:c.3350-62_3350-61dup (MSH6)	ENSP00000390382.2:n.3350-62_3350-61dup
ENST00000455383.6:c.3350-62_3350-61dup (MSH6)	ENSP00000397484.2:n.3350-62_3350-61dup
ENST00000700004.2:c.3263-62_3263-61dup (MSH6)	ENSP00000514752.2:n.3263-62_3263-61dup
ENST00000699999.1:n.4321-62_4321-61dup (MSH6)
ENST00000700000.1:c.2081-62_2081-61dup (MSH6)	ENSP00000514749.1:n.2081-62_2081-61dup
ENST00000700002.1:c.3653-62_3653-61dup (MSH6)	ENSP00000514750.1:n.3653-62_3653-61dup
ENST00000700003.1:c.1102-62_1102-61dup (MSH6)	ENSP00000514751.1:n.1102-62_1102-61dup
ENST00000700004.1:c.2420-62_2420-61dup (MSH6)	ENSP00000514752.1:n.2420-62_2420-61dup
ENST00000700005.1:n.2498-62_2498-61dup (MSH6)
ENST00000700006.1:n.4743_4744dup (MSH6)
ENST00000700007.1:n.2242-62_2242-61dup (MSH6)
ENST00000700008.1:n.1816-62_1816-61dup (MSH6)
ENST00000700009.1:n.2249_2250dup (MSH6)
ENST00000700010.1:n.1056-62_1056-61dup (MSH6)
ENST00000700011.1:n.2941-62_2941-61dup (MSH6)
ENST00000682451.1:n.4607_4608dup (FBXO11)
ENST00000684712.1:n.4869_4870dup (FBXO11)
ENST00000234420.11:c.3647-62_3647-61dup (MSH6) MANE Select	ENSP00000234420.5:n.3647-62_3647-61dup
ENST00000540021.6:c.3257-62_3257-61dup (MSH6)	ENSP00000446475.1:n.3257-62_3257-61dup
ENST00000652107.1:c.3350-62_3350-61dup (MSH6)	ENSP00000498629.1:n.3350-62_3350-61dup
ENST00000673637.1:c.3350-62_3350-61dup (MSH6)	ENSP00000501310.1:n.3350-62_3350-61dup
ENST00000234420.9:c.3647-62_3647-61dup (MSH6)	ENSP00000234420.4:n.3647-62_3647-61dup
ENST00000405808.5:c.169+2054_169+2055dup (FBXO11)	ENSP00000385127.1:n.169+2054_169+2055dup
ENST00000434234.5:c.*124+1853_*124+1854dup (FBXO11)	ENSP00000402692.1:n.*124+1853_*124+1854dup
ENST00000445503.5:c.*2994-62_*2994-61dup (MSH6)	ENSP00000405294.1:n.*2994-62_*2994-61dup
ENST00000538136.1:c.2741-62_2741-61dup (MSH6)	ENSP00000438580.1:n.2741-62_2741-61dup
ENST00000540021.5:c.3257-62_3257-61dup (MSH6)	ENSP00000446475.1:n.3257-62_3257-61dup
ENST00000614496.4:c.2741-62_2741-61dup (MSH6)	ENSP00000477844.1:n.2741-62_2741-61dup
ENST00000622629.4:c.551-62_551-61dup (MSH6)	ENSP00000482078.1:n.551-62_551-61dup
NM_000179.2:c.3647-62_3647-61dup , LRG_219t1:c.3647-62_3647-61dup (MSH6)	NP_000170.1:n.3647-62_3647-61dup
NM_001281492.1:c.3257-62_3257-61dup (MSH6)	NP_001268421.1:n.3257-62_3257-61dup
NM_001281493.1:c.2741-62_2741-61dup (MSH6)	NP_001268422.1:n.2741-62_2741-61dup
NM_001281494.1:c.2741-62_2741-61dup (MSH6)	NP_001268423.1:n.2741-62_2741-61dup
XM_005264271.1:c.3350-62_3350-61dup (MSH6)	XP_005264328.1:n.3350-62_3350-61dup
XM_011532798.1:c.3464-62_3464-61dup (MSH6)	XP_011531100.1:n.3464-62_3464-61dup
XM_011532799.1:c.3350-62_3350-61dup (MSH6)	XP_011531101.1:n.3350-62_3350-61dup
XM_011532800.1:c.3350-62_3350-61dup (MSH6)	XP_011531102.1:n.3350-62_3350-61dup
XM_024452819.1:c.3647-62_3647-61dup (MSH6)	XP_024308587.1:n.3647-62_3647-61dup
XM_024452820.1:c.3464-62_3464-61dup (MSH6)	XP_024308588.1:n.3464-62_3464-61dup
XM_024452821.1:c.3350-62_3350-61dup (MSH6)	XP_024308589.1:n.3350-62_3350-61dup
XM_024452822.1:c.2741-62_2741-61dup (MSH6)	XP_024308590.1:n.2741-62_2741-61dup
NM_000179.3:c.3647-62_3647-61dup (MSH6) MANE Select	NP_000170.1:n.3647-62_3647-61dup
NM_001281492.2:c.3257-62_3257-61dup (MSH6)	NP_001268421.1:n.3257-62_3257-61dup
NM_001281493.2:c.2741-62_2741-61dup (MSH6)	NP_001268422.1:n.2741-62_2741-61dup
NM_001281494.2:c.2741-62_2741-61dup (MSH6)	NP_001268423.1:n.2741-62_2741-61dup