Canonical Allele Identifier: CA2496049444

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800398_47800401delinsCTCC , CM000664.2:g.47800398_47800401delinsCTCC	GRCh38
NC_000002.11:g.48027537_48027540delinsCTCC , CM000664.1:g.48027537_48027540delinsCTCC	GRCh37
NC_000002.10:g.47881041_47881044delinsCTCC	NCBI36
NG_007111.1:g.22252_22255delinsCTCC , LRG_219:g.22252_22255delinsCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2118_2121delinsCTCC (MSH6)	ENSP00000406248.2:p.Ile706=
ENST00000420813.6:c.2118_2121delinsCTCC (MSH6)	ENSP00000390382.2:p.Ile706=
ENST00000455383.6:c.2118_2121delinsCTCC (MSH6)	ENSP00000397484.2:p.Ile706=
ENST00000700004.2:c.2415_2418delinsCTCC (MSH6)	ENSP00000514752.2:p.Ile805=
ENST00000699999.1:n.2499_2502delinsCTCC (MSH6)
ENST00000700000.1:c.1606+809_1606+812delinsCTCC (MSH6)	ENSP00000514749.1:n.1606+809_1606+812delinsCTCC
ENST00000700002.1:c.2421_2424delinsCTCC (MSH6)	ENSP00000514750.1:p.Ile807=
ENST00000700003.1:c.628-3022_628-3019delinsCTCC (MSH6)	ENSP00000514751.1:n.628-3022_628-3019delinsCTCC
ENST00000700004.1:c.1572_1575delinsCTCC (MSH6)	ENSP00000514752.1:p.Ile524=
ENST00000234420.11:c.2415_2418delinsCTCC (MSH6) MANE Select	ENSP00000234420.5:p.Ile805=
ENST00000540021.6:c.2025_2028delinsCTCC (MSH6)	ENSP00000446475.1:p.Ile675=
ENST00000652107.1:c.2118_2121delinsCTCC (MSH6)	ENSP00000498629.1:p.Ile706=
ENST00000673637.1:c.2118_2121delinsCTCC (MSH6)	ENSP00000501310.1:p.Ile706=
ENST00000234420.9:c.2415_2418delinsCTCC (MSH6)	ENSP00000234420.4:p.Ile805=
ENST00000405808.5:c.169+7794_169+7797delinsGGAG (FBXO11)	ENSP00000385127.1:n.169+7794_169+7797delinsGGAG
ENST00000434234.5:c.*124+7593_*124+7596delinsGGAG (FBXO11)	ENSP00000402692.1:n.*124+7593_*124+7596delinsGGAG
ENST00000445503.5:c.*1762_*1765delinsCTCC (MSH6)	ENSP00000405294.1:n.*1762_*1765delinsCTCC
ENST00000538136.1:c.1509_1512delinsCTCC (MSH6)	ENSP00000438580.1:p.Ile503=
ENST00000540021.5:c.2025_2028delinsCTCC (MSH6)	ENSP00000446475.1:p.Ile675=
ENST00000614496.4:c.1509_1512delinsCTCC (MSH6)	ENSP00000477844.1:p.Ile503=
ENST00000616033.4:c.2412_2415delinsCTCC (MSH6)	ENSP00000480261.1:p.Ile804=
ENST00000622629.4:c.-682_-679delinsCTCC (MSH6)	ENSP00000482078.1:n.-682_-679delinsCTCC
NM_000179.2:c.2415_2418delinsCTCC , LRG_219t1:c.2415_2418delinsCTCC (MSH6)	NP_000170.1:p.Ile805=
NM_001281492.1:c.2025_2028delinsCTCC (MSH6)	NP_001268421.1:p.Ile675=
NM_001281493.1:c.1509_1512delinsCTCC (MSH6)	NP_001268422.1:p.Ile503=
NM_001281494.1:c.1509_1512delinsCTCC (MSH6)	NP_001268423.1:p.Ile503=
XM_005264271.1:c.2118_2121delinsCTCC (MSH6)	XP_005264328.1:p.Ile706=
XM_011532798.1:c.2232_2235delinsCTCC (MSH6)	XP_011531100.1:p.Ile744=
XM_011532799.1:c.2118_2121delinsCTCC (MSH6)	XP_011531101.1:p.Ile706=
XM_011532800.1:c.2118_2121delinsCTCC (MSH6)	XP_011531102.1:p.Ile706=
XM_024452819.1:c.2415_2418delinsCTCC (MSH6)	XP_024308587.1:p.Ile805=
XM_024452820.1:c.2232_2235delinsCTCC (MSH6)	XP_024308588.1:p.Ile744=
XM_024452821.1:c.2118_2121delinsCTCC (MSH6)	XP_024308589.1:p.Ile706=
XM_024452822.1:c.1509_1512delinsCTCC (MSH6)	XP_024308590.1:p.Ile503=
NM_000179.3:c.2415_2418delinsCTCC (MSH6) MANE Select	NP_000170.1:p.Ile805=
NM_001281492.2:c.2025_2028delinsCTCC (MSH6)	NP_001268421.1:p.Ile675=
NM_001281493.2:c.1509_1512delinsCTCC (MSH6)	NP_001268422.1:p.Ile503=
NM_001281494.2:c.1509_1512delinsCTCC (MSH6)	NP_001268423.1:p.Ile503=