Canonical Allele Identifier: CA2838032280

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799485_47800253del , CM000664.2:g.47799485_47800253del	GRCh38
NC_000002.11:g.48026624_48027392del , CM000664.1:g.48026624_48027392del	GRCh37
NC_000002.10:g.47880128_47880896del	NCBI36
NG_007111.1:g.21339_22107del , LRG_219:g.21339_22107del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1205_1973del (MSH6)	ENSP00000406248.2:p.His402ProfsTer3
ENST00000420813.6:c.1205_1973del (MSH6)	ENSP00000390382.2:p.His402ProfsTer3
ENST00000455383.6:c.1205_1973del (MSH6)	ENSP00000397484.2:p.His402ProfsTer3
ENST00000700004.2:c.1502_2270del (MSH6)	ENSP00000514752.2:p.His501ProfsTer3
ENST00000699999.1:n.1586_2354del (MSH6)
ENST00000700000.1:c.1502_1606+664del (MSH6)
ENST00000700002.1:c.1508_2276del (MSH6)	ENSP00000514750.1:p.His503ProfsTer3
ENST00000700003.1:c.627+3422_628-3167del (MSH6)	ENSP00000514751.1:n.627+3422_628-3167del
ENST00000700004.1:c.659_1427del (MSH6)	ENSP00000514752.1:p.His220ProfsTer3
ENST00000234420.11:c.1502_2270del (MSH6) MANE Select	ENSP00000234420.5:p.His501ProfsTer3
ENST00000540021.6:c.1112_1880del (MSH6)	ENSP00000446475.1:p.His371ProfsTer3
ENST00000652107.1:c.1205_1973del (MSH6)	ENSP00000498629.1:p.His402ProfsTer3
ENST00000673637.1:c.1205_1973del (MSH6)	ENSP00000501310.1:p.His402ProfsTer3
ENST00000234420.9:c.1502_2270del (MSH6)	ENSP00000234420.4:p.His501ProfsTer3
ENST00000405808.5:c.169+7944_169+8712del (FBXO11)	ENSP00000385127.1:n.169+7944_169+8712del
ENST00000434234.5:c.*124+7743_*124+8511del (FBXO11)	ENSP00000402692.1:n.*124+7743_*124+8511del
ENST00000445503.5:c.*849_*1617del (MSH6)	ENSP00000405294.1:n.*849_*1617del
ENST00000538136.1:c.596_1364del (MSH6)	ENSP00000438580.1:p.His199ProfsTer3
ENST00000540021.5:c.1112_1880del (MSH6)	ENSP00000446475.1:p.His371ProfsTer3
ENST00000614496.4:c.596_1364del (MSH6)	ENSP00000477844.1:p.His199ProfsTer3
ENST00000616033.4:c.1499_2267del (MSH6)	ENSP00000480261.1:p.His500ProfsTer3
ENST00000622629.4:c.-1595_-827del (MSH6)	ENSP00000482078.1:n.-1595_-827del
NM_000179.2:c.1502_2270del , LRG_219t1:c.1502_2270del (MSH6)	NP_000170.1:p.His501ProfsTer3
NM_001281492.1:c.1112_1880del (MSH6)	NP_001268421.1:p.His371ProfsTer3
NM_001281493.1:c.596_1364del (MSH6)	NP_001268422.1:p.His199ProfsTer3
NM_001281494.1:c.596_1364del (MSH6)	NP_001268423.1:p.His199ProfsTer3
XM_005264271.1:c.1205_1973del (MSH6)	XP_005264328.1:p.His402ProfsTer3
XM_011532798.1:c.1319_2087del (MSH6)	XP_011531100.1:p.His440ProfsTer3
XM_011532799.1:c.1205_1973del (MSH6)	XP_011531101.1:p.His402ProfsTer3
XM_011532800.1:c.1205_1973del (MSH6)	XP_011531102.1:p.His402ProfsTer3
XM_024452819.1:c.1502_2270del (MSH6)	XP_024308587.1:p.His501ProfsTer3
XM_024452820.1:c.1319_2087del (MSH6)	XP_024308588.1:p.His440ProfsTer3
XM_024452821.1:c.1205_1973del (MSH6)	XP_024308589.1:p.His402ProfsTer3
XM_024452822.1:c.596_1364del (MSH6)	XP_024308590.1:p.His199ProfsTer3
NM_000179.3:c.1502_2270del (MSH6) MANE Select	NP_000170.1:p.His501ProfsTer3
NM_001281492.2:c.1112_1880del (MSH6)	NP_001268421.1:p.His371ProfsTer3
NM_001281493.2:c.596_1364del (MSH6)	NP_001268422.1:p.His199ProfsTer3
NM_001281494.2:c.596_1364del (MSH6)	NP_001268423.1:p.His199ProfsTer3