Canonical Allele Identifier: CA2580067798

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1788018
• ClinVar RCV Id: RCV002428163

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800211_47800212insAT , CM000664.2:g.47800211_47800212insAT	GRCh38
NC_000002.11:g.48027350_48027351insAT , CM000664.1:g.48027350_48027351insAT	GRCh37
NC_000002.10:g.47880854_47880855insAT	NCBI36
NG_007111.1:g.22065_22066insAT , LRG_219:g.22065_22066insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1931_1932insAT (MSH6)	ENSP00000406248.2:p.Glu645TrpfsTer5
ENST00000420813.6:c.1931_1932insAT (MSH6)	ENSP00000390382.2:p.Glu645TrpfsTer5
ENST00000455383.6:c.1931_1932insAT (MSH6)	ENSP00000397484.2:p.Glu645TrpfsTer5
ENST00000700004.2:c.2228_2229insAT (MSH6)	ENSP00000514752.2:p.Glu744TrpfsTer5
ENST00000699999.1:n.2312_2313insAT (MSH6)
ENST00000700000.1:c.1606+622_1606+623insAT (MSH6)	ENSP00000514749.1:n.1606+622_1606+623insAT
ENST00000700002.1:c.2234_2235insAT (MSH6)	ENSP00000514750.1:p.Glu746TrpfsTer5
ENST00000700003.1:c.628-3209_628-3208insAT (MSH6)	ENSP00000514751.1:n.628-3209_628-3208insAT
ENST00000700004.1:c.1385_1386insAT (MSH6)	ENSP00000514752.1:p.Glu463TrpfsTer5
ENST00000234420.11:c.2228_2229insAT (MSH6) MANE Select	ENSP00000234420.5:p.Glu744TrpfsTer5
ENST00000540021.6:c.1838_1839insAT (MSH6)	ENSP00000446475.1:p.Glu614TrpfsTer5
ENST00000652107.1:c.1931_1932insAT (MSH6)	ENSP00000498629.1:p.Glu645TrpfsTer5
ENST00000673637.1:c.1931_1932insAT (MSH6)	ENSP00000501310.1:p.Glu645TrpfsTer5
ENST00000234420.9:c.2228_2229insAT (MSH6)	ENSP00000234420.4:p.Glu744TrpfsTer5
ENST00000405808.5:c.169+7984_169+7985insTA (FBXO11)	ENSP00000385127.1:n.169+7984_169+7985insTA
ENST00000434234.5:c.*124+7783_*124+7784insTA (FBXO11)	ENSP00000402692.1:n.*124+7783_*124+7784insTA
ENST00000445503.5:c.*1575_*1576insAT (MSH6)	ENSP00000405294.1:n.*1575_*1576insAT
ENST00000538136.1:c.1322_1323insAT (MSH6)	ENSP00000438580.1:p.Glu442TrpfsTer5
ENST00000540021.5:c.1838_1839insAT (MSH6)	ENSP00000446475.1:p.Glu614TrpfsTer5
ENST00000614496.4:c.1322_1323insAT (MSH6)	ENSP00000477844.1:p.Glu442TrpfsTer5
ENST00000616033.4:c.2225_2226insAT (MSH6)	ENSP00000480261.1:p.Glu743TrpfsTer5
ENST00000622629.4:c.-869_-868insAT (MSH6)	ENSP00000482078.1:n.-869_-868insAT
NM_000179.2:c.2228_2229insAT , LRG_219t1:c.2228_2229insAT (MSH6)	NP_000170.1:p.Glu744TrpfsTer5
NM_001281492.1:c.1838_1839insAT (MSH6)	NP_001268421.1:p.Glu614TrpfsTer5
NM_001281493.1:c.1322_1323insAT (MSH6)	NP_001268422.1:p.Glu442TrpfsTer5
NM_001281494.1:c.1322_1323insAT (MSH6)	NP_001268423.1:p.Glu442TrpfsTer5
XM_005264271.1:c.1931_1932insAT (MSH6)	XP_005264328.1:p.Glu645TrpfsTer5
XM_011532798.1:c.2045_2046insAT (MSH6)	XP_011531100.1:p.Glu683TrpfsTer5
XM_011532799.1:c.1931_1932insAT (MSH6)	XP_011531101.1:p.Glu645TrpfsTer5
XM_011532800.1:c.1931_1932insAT (MSH6)	XP_011531102.1:p.Glu645TrpfsTer5
XM_024452819.1:c.2228_2229insAT (MSH6)	XP_024308587.1:p.Glu744TrpfsTer5
XM_024452820.1:c.2045_2046insAT (MSH6)	XP_024308588.1:p.Glu683TrpfsTer5
XM_024452821.1:c.1931_1932insAT (MSH6)	XP_024308589.1:p.Glu645TrpfsTer5
XM_024452822.1:c.1322_1323insAT (MSH6)	XP_024308590.1:p.Glu442TrpfsTer5
NM_000179.3:c.2228_2229insAT (MSH6) MANE Select	NP_000170.1:p.Glu744TrpfsTer5
NM_001281492.2:c.1838_1839insAT (MSH6)	NP_001268421.1:p.Glu614TrpfsTer5
NM_001281493.2:c.1322_1323insAT (MSH6)	NP_001268422.1:p.Glu442TrpfsTer5
NM_001281494.2:c.1322_1323insAT (MSH6)	NP_001268423.1:p.Glu442TrpfsTer5