Canonical Allele Identifier: CA2496043094

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47790765_47790766delinsCA , CM000664.2:g.47790765_47790766delinsCA	GRCh38
NC_000002.11:g.48017904_48017905delinsCA , CM000664.1:g.48017904_48017905delinsCA	GRCh37
NC_000002.10:g.47871408_47871409delinsCA	NCBI36
NG_007111.1:g.12619_12620delinsCA , LRG_219:g.12619_12620delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000406248.2:n.-37-162_-37-161delinsCA
ENST00000420813.6:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000390382.2:n.-37-162_-37-161delinsCA
ENST00000455383.6:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000397484.2:n.-37-162_-37-161delinsCA
ENST00000700004.2:c.261-162_261-161delinsCA (MSH6)	ENSP00000514752.2:n.261-162_261-161delinsCA
ENST00000699999.1:n.345-162_345-161delinsCA (MSH6)
ENST00000700000.1:c.261-162_261-161delinsCA (MSH6)	ENSP00000514749.1:n.261-162_261-161delinsCA
ENST00000700001.1:n.333-162_333-161delinsCA (MSH6)
ENST00000700002.1:c.261-162_261-161delinsCA (MSH6)	ENSP00000514750.1:n.261-162_261-161delinsCA
ENST00000700003.1:c.261-162_261-161delinsCA (MSH6)	ENSP00000514751.1:n.261-162_261-161delinsCA
ENST00000234420.11:c.261-162_261-161delinsCA (MSH6) MANE Select	ENSP00000234420.5:n.261-162_261-161delinsCA
ENST00000540021.6:c.237+7295_237+7296delinsCA (MSH6)	ENSP00000446475.1:n.237+7295_237+7296delinsCA
ENST00000652107.1:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000498629.1:n.-37-162_-37-161delinsCA
ENST00000673637.1:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000501310.1:n.-37-162_-37-161delinsCA
ENST00000673922.1:n.349+7272_349+7273delinsCA (MSH6)
ENST00000234420.9:c.261-162_261-161delinsCA (MSH6)	ENSP00000234420.4:n.261-162_261-161delinsCA
ENST00000405808.5:c.170-1326_170-1325delinsTG (FBXO11)	ENSP00000385127.1:n.170-1326_170-1325delinsTG
ENST00000411819.1:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000406248.1:n.-37-162_-37-161delinsCA
ENST00000420813.5:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000390382.1:n.-37-162_-37-161delinsCA
ENST00000434234.5:c.*125-1326_*125-1325delinsTG (FBXO11)	ENSP00000402692.1:n.*125-1326_*125-1325delinsTG
ENST00000445503.5:c.261-162_261-161delinsCA (MSH6)	ENSP00000405294.1:n.261-162_261-161delinsCA
ENST00000455383.5:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000397484.1:n.-37-162_-37-161delinsCA
ENST00000456246.1:c.261-5129_261-5128delinsCA (MSH6)	ENSP00000410570.1:n.261-5129_261-5128delinsCA
ENST00000538136.1:c.-642-162_-642-161delinsCA (MSH6)	ENSP00000438580.1:n.-642-162_-642-161delinsCA
ENST00000540021.5:c.237+7295_237+7296delinsCA (MSH6)	ENSP00000446475.1:n.237+7295_237+7296delinsCA
ENST00000606499.1:c.-37-162_-37-161delinsCA (MSH6)	ENSP00000475605.1:n.-37-162_-37-161delinsCA
ENST00000614496.4:c.-476-162_-476-161delinsCA (MSH6)	ENSP00000477844.1:n.-476-162_-476-161delinsCA
ENST00000616033.4:c.258-162_258-161delinsCA (MSH6)	ENSP00000480261.1:n.258-162_258-161delinsCA
ENST00000622629.4:c.-2836-162_-2836-161delinsCA (MSH6)	ENSP00000482078.1:n.-2836-162_-2836-161delinsCA
NM_000179.2:c.261-162_261-161delinsCA , LRG_219t1:c.261-162_261-161delinsCA (MSH6)	NP_000170.1:n.261-162_261-161delinsCA
NM_001281492.1:c.237+7295_237+7296delinsCA (MSH6)	NP_001268421.1:n.237+7295_237+7296delinsCA
NM_001281493.1:c.-476-162_-476-161delinsCA (MSH6)	NP_001268422.1:n.-476-162_-476-161delinsCA
NM_001281494.1:c.-642-162_-642-161delinsCA (MSH6)	NP_001268423.1:n.-642-162_-642-161delinsCA
XM_005264271.1:c.-37-162_-37-161delinsCA (MSH6)	XP_005264328.1:n.-37-162_-37-161delinsCA
XM_011532798.1:c.78-162_78-161delinsCA (MSH6)	XP_011531100.1:n.78-162_78-161delinsCA
XM_011532799.1:c.-37-162_-37-161delinsCA (MSH6)	XP_011531101.1:n.-37-162_-37-161delinsCA
XM_011532800.1:c.-37-162_-37-161delinsCA (MSH6)	XP_011531102.1:n.-37-162_-37-161delinsCA
XM_024452819.1:c.261-162_261-161delinsCA (MSH6)	XP_024308587.1:n.261-162_261-161delinsCA
XM_024452820.1:c.78-162_78-161delinsCA (MSH6)	XP_024308588.1:n.78-162_78-161delinsCA
XM_024452821.1:c.-37-162_-37-161delinsCA (MSH6)	XP_024308589.1:n.-37-162_-37-161delinsCA
XM_024452822.1:c.-476-162_-476-161delinsCA (MSH6)	XP_024308590.1:n.-476-162_-476-161delinsCA
NM_000179.3:c.261-162_261-161delinsCA (MSH6) MANE Select	NP_000170.1:n.261-162_261-161delinsCA
NM_001281492.2:c.237+7295_237+7296delinsCA (MSH6)	NP_001268421.1:n.237+7295_237+7296delinsCA
NM_001281493.2:c.-476-162_-476-161delinsCA (MSH6)	NP_001268422.1:n.-476-162_-476-161delinsCA
NM_001281494.2:c.-642-162_-642-161delinsCA (MSH6)	NP_001268423.1:n.-642-162_-642-161delinsCA