Canonical Allele Identifier: CA2496049465

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800409_47800420delinsTAGAGCTTCTAA , CM000664.2:g.47800409_47800420delinsTAGAGCTTCTAA	GRCh38
NC_000002.11:g.48027548_48027559delinsTAGAGCTTCTAA , CM000664.1:g.48027548_48027559delinsTAGAGCTTCTAA	GRCh37
NC_000002.10:g.47881052_47881063delinsTAGAGCTTCTAA	NCBI36
NG_007111.1:g.22263_22274delinsTAGAGCTTCTAA , LRG_219:g.22263_22274delinsTAGAGCTTCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	ENSP00000406248.2:p.Val710=
ENST00000420813.6:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	ENSP00000390382.2:p.Val710=
ENST00000455383.6:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	ENSP00000397484.2:p.Val710=
ENST00000700004.2:c.2426_2437delinsTAGAGCTTCTAA (MSH6)	ENSP00000514752.2:p.Val809=
ENST00000699999.1:n.2510_2521delinsTAGAGCTTCTAA (MSH6)
ENST00000700000.1:c.1606+820_1606+831delinsTAGAGCTTCTAA (MSH6)	ENSP00000514749.1:n.1606+820_1606+831delinsTAGAGCTTCTAA
ENST00000700002.1:c.2432_2443delinsTAGAGCTTCTAA (MSH6)	ENSP00000514750.1:p.Val811=
ENST00000700003.1:c.628-3011_628-3000delinsTAGAGCTTCTAA (MSH6)	ENSP00000514751.1:n.628-3011_628-3000delinsTAGAGCTTCTAA
ENST00000700004.1:c.1583_1594delinsTAGAGCTTCTAA (MSH6)	ENSP00000514752.1:p.Val528=
ENST00000234420.11:c.2426_2437delinsTAGAGCTTCTAA (MSH6) MANE Select	ENSP00000234420.5:p.Val809=
ENST00000540021.6:c.2036_2047delinsTAGAGCTTCTAA (MSH6)	ENSP00000446475.1:p.Val679=
ENST00000652107.1:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	ENSP00000498629.1:p.Val710=
ENST00000673637.1:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	ENSP00000501310.1:p.Val710=
ENST00000234420.9:c.2426_2437delinsTAGAGCTTCTAA (MSH6)	ENSP00000234420.4:p.Val809=
ENST00000405808.5:c.169+7775_169+7786delinsTTAGAAGCTCTA (FBXO11)	ENSP00000385127.1:n.169+7775_169+7786delinsTTAGAAGCTCTA
ENST00000434234.5:c.*124+7574_*124+7585delinsTTAGAAGCTCTA (FBXO11)	ENSP00000402692.1:n.*124+7574_*124+7585delinsTTAGAAGCTCTA
ENST00000445503.5:c.*1773_*1784delinsTAGAGCTTCTAA (MSH6)	ENSP00000405294.1:n.*1773_*1784delinsTAGAGCTTCTAA
ENST00000538136.1:c.1520_1531delinsTAGAGCTTCTAA (MSH6)	ENSP00000438580.1:p.Val507=
ENST00000540021.5:c.2036_2047delinsTAGAGCTTCTAA (MSH6)	ENSP00000446475.1:p.Val679=
ENST00000614496.4:c.1520_1531delinsTAGAGCTTCTAA (MSH6)	ENSP00000477844.1:p.Val507=
ENST00000616033.4:c.2423_2434delinsTAGAGCTTCTAA (MSH6)	ENSP00000480261.1:p.Val808=
ENST00000622629.4:c.-671_-660delinsTAGAGCTTCTAA (MSH6)	ENSP00000482078.1:n.-671_-660delinsTAGAGCTTCTAA
NM_000179.2:c.2426_2437delinsTAGAGCTTCTAA , LRG_219t1:c.2426_2437delinsTAGAGCTTCTAA (MSH6)	NP_000170.1:p.Val809=
NM_001281492.1:c.2036_2047delinsTAGAGCTTCTAA (MSH6)	NP_001268421.1:p.Val679=
NM_001281493.1:c.1520_1531delinsTAGAGCTTCTAA (MSH6)	NP_001268422.1:p.Val507=
NM_001281494.1:c.1520_1531delinsTAGAGCTTCTAA (MSH6)	NP_001268423.1:p.Val507=
XM_005264271.1:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	XP_005264328.1:p.Val710=
XM_011532798.1:c.2243_2254delinsTAGAGCTTCTAA (MSH6)	XP_011531100.1:p.Val748=
XM_011532799.1:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	XP_011531101.1:p.Val710=
XM_011532800.1:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	XP_011531102.1:p.Val710=
XM_024452819.1:c.2426_2437delinsTAGAGCTTCTAA (MSH6)	XP_024308587.1:p.Val809=
XM_024452820.1:c.2243_2254delinsTAGAGCTTCTAA (MSH6)	XP_024308588.1:p.Val748=
XM_024452821.1:c.2129_2140delinsTAGAGCTTCTAA (MSH6)	XP_024308589.1:p.Val710=
XM_024452822.1:c.1520_1531delinsTAGAGCTTCTAA (MSH6)	XP_024308590.1:p.Val507=
NM_000179.3:c.2426_2437delinsTAGAGCTTCTAA (MSH6) MANE Select	NP_000170.1:p.Val809=
NM_001281492.2:c.2036_2047delinsTAGAGCTTCTAA (MSH6)	NP_001268421.1:p.Val679=
NM_001281493.2:c.1520_1531delinsTAGAGCTTCTAA (MSH6)	NP_001268422.1:p.Val507=
NM_001281494.2:c.1520_1531delinsTAGAGCTTCTAA (MSH6)	NP_001268423.1:p.Val507=