Canonical Allele Identifier: CA2695200657

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 2673771
• ClinVar RCV Id: RCV003450408

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799958_47799959insCT , CM000664.2:g.47799958_47799959insCT	GRCh38
NC_000002.11:g.48027097_48027098insCT , CM000664.1:g.48027097_48027098insCT	GRCh37
NC_000002.10:g.47880601_47880602insCT	NCBI36
NG_007111.1:g.21812_21813insCT , LRG_219:g.21812_21813insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1678_1679insCT (MSH6)	ENSP00000406248.2:p.Leu560ProfsTer5
ENST00000420813.6:c.1678_1679insCT (MSH6)	ENSP00000390382.2:p.Leu560ProfsTer5
ENST00000455383.6:c.1678_1679insCT (MSH6)	ENSP00000397484.2:p.Leu560ProfsTer5
ENST00000700004.2:c.1975_1976insCT (MSH6)	ENSP00000514752.2:p.Leu659ProfsTer5
ENST00000699999.1:n.2059_2060insCT (MSH6)
ENST00000700000.1:c.1606+369_1606+370insCT (MSH6)	ENSP00000514749.1:n.1606+369_1606+370insCT
ENST00000700002.1:c.1981_1982insCT (MSH6)	ENSP00000514750.1:p.Leu661ProfsTer5
ENST00000700003.1:c.628-3462_628-3461insCT (MSH6)	ENSP00000514751.1:n.628-3462_628-3461insCT
ENST00000700004.1:c.1132_1133insCT (MSH6)	ENSP00000514752.1:p.Leu378ProfsTer5
ENST00000234420.11:c.1975_1976insCT (MSH6) MANE Select	ENSP00000234420.5:p.Leu659ProfsTer5
ENST00000540021.6:c.1585_1586insCT (MSH6)	ENSP00000446475.1:p.Leu529ProfsTer5
ENST00000652107.1:c.1678_1679insCT (MSH6)	ENSP00000498629.1:p.Leu560ProfsTer5
ENST00000673637.1:c.1678_1679insCT (MSH6)	ENSP00000501310.1:p.Leu560ProfsTer5
ENST00000234420.9:c.1975_1976insCT (MSH6)	ENSP00000234420.4:p.Leu659ProfsTer5
ENST00000405808.5:c.169+8236_169+8237insAG (FBXO11)	ENSP00000385127.1:n.169+8236_169+8237insAG
ENST00000434234.5:c.*124+8035_*124+8036insAG (FBXO11)	ENSP00000402692.1:n.*124+8035_*124+8036insAG
ENST00000445503.5:c.*1322_*1323insCT (MSH6)	ENSP00000405294.1:n.*1322_*1323insCT
ENST00000538136.1:c.1069_1070insCT (MSH6)	ENSP00000438580.1:p.Leu357ProfsTer5
ENST00000540021.5:c.1585_1586insCT (MSH6)	ENSP00000446475.1:p.Leu529ProfsTer5
ENST00000614496.4:c.1069_1070insCT (MSH6)	ENSP00000477844.1:p.Leu357ProfsTer5
ENST00000616033.4:c.1972_1973insCT (MSH6)	ENSP00000480261.1:p.Leu658ProfsTer5
ENST00000622629.4:c.-1122_-1121insCT (MSH6)	ENSP00000482078.1:n.-1122_-1121insCT
NM_000179.2:c.1975_1976insCT , LRG_219t1:c.1975_1976insCT (MSH6)	NP_000170.1:p.Leu659ProfsTer5
NM_001281492.1:c.1585_1586insCT (MSH6)	NP_001268421.1:p.Leu529ProfsTer5
NM_001281493.1:c.1069_1070insCT (MSH6)	NP_001268422.1:p.Leu357ProfsTer5
NM_001281494.1:c.1069_1070insCT (MSH6)	NP_001268423.1:p.Leu357ProfsTer5
XM_005264271.1:c.1678_1679insCT (MSH6)	XP_005264328.1:p.Leu560ProfsTer5
XM_011532798.1:c.1792_1793insCT (MSH6)	XP_011531100.1:p.Leu598ProfsTer5
XM_011532799.1:c.1678_1679insCT (MSH6)	XP_011531101.1:p.Leu560ProfsTer5
XM_011532800.1:c.1678_1679insCT (MSH6)	XP_011531102.1:p.Leu560ProfsTer5
XM_024452819.1:c.1975_1976insCT (MSH6)	XP_024308587.1:p.Leu659ProfsTer5
XM_024452820.1:c.1792_1793insCT (MSH6)	XP_024308588.1:p.Leu598ProfsTer5
XM_024452821.1:c.1678_1679insCT (MSH6)	XP_024308589.1:p.Leu560ProfsTer5
XM_024452822.1:c.1069_1070insCT (MSH6)	XP_024308590.1:p.Leu357ProfsTer5
NM_000179.3:c.1975_1976insCT (MSH6) MANE Select	NP_000170.1:p.Leu659ProfsTer5
NM_001281492.2:c.1585_1586insCT (MSH6)	NP_001268421.1:p.Leu529ProfsTer5
NM_001281493.2:c.1069_1070insCT (MSH6)	NP_001268422.1:p.Leu357ProfsTer5
NM_001281494.2:c.1069_1070insCT (MSH6)	NP_001268423.1:p.Leu357ProfsTer5