Canonical Allele Identifier: CA658795770

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 525640
• ClinVar RCV Id: RCV000629769 ; RCV000759852 ; RCV001193096 ; RCV003451485
• dbSNP Id: rs1553413640
• MyVariant Identifiers: chr2:g.48027382dup (hg19) ; chr2:g.47800243dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800243dup , CM000664.2:g.47800243dup	GRCh38
NC_000002.11:g.48027382dup , CM000664.1:g.48027382dup	GRCh37
NC_000002.10:g.47880886dup	NCBI36
NG_007111.1:g.22097dup , LRG_219:g.22097dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1963dup (MSH6)	ENSP00000406248.2:p.Thr655AsnfsTer2
ENST00000420813.6:c.1963dup (MSH6)	ENSP00000390382.2:p.Thr655AsnfsTer2
ENST00000455383.6:c.1963dup (MSH6)	ENSP00000397484.2:p.Thr655AsnfsTer2
ENST00000700004.2:c.2260dup (MSH6)	ENSP00000514752.2:p.Thr754AsnfsTer2
ENST00000699999.1:n.2344dup (MSH6)
ENST00000700000.1:c.1606+654dup (MSH6)	ENSP00000514749.1:n.1606+654dup
ENST00000700002.1:c.2266dup (MSH6)	ENSP00000514750.1:p.Thr756AsnfsTer2
ENST00000700003.1:c.628-3177dup (MSH6)	ENSP00000514751.1:n.628-3177dup
ENST00000700004.1:c.1417dup (MSH6)	ENSP00000514752.1:p.Thr473AsnfsTer2
ENST00000234420.11:c.2260dup (MSH6) MANE Select	ENSP00000234420.5:p.Thr754AsnfsTer2
ENST00000540021.6:c.1870dup (MSH6)	ENSP00000446475.1:p.Thr624AsnfsTer2
ENST00000652107.1:c.1963dup (MSH6)	ENSP00000498629.1:p.Thr655AsnfsTer2
ENST00000673637.1:c.1963dup (MSH6)	ENSP00000501310.1:p.Thr655AsnfsTer2
ENST00000234420.9:c.2260dup (MSH6)	ENSP00000234420.4:p.Thr754AsnfsTer2
ENST00000405808.5:c.169+7952dup (FBXO11)	ENSP00000385127.1:n.169+7952dup
ENST00000434234.5:c.*124+7751dup (FBXO11)	ENSP00000402692.1:n.*124+7751dup
ENST00000445503.5:c.*1607dup (MSH6)	ENSP00000405294.1:n.*1607dup
ENST00000538136.1:c.1354dup (MSH6)	ENSP00000438580.1:p.Thr452AsnfsTer2
ENST00000540021.5:c.1870dup (MSH6)	ENSP00000446475.1:p.Thr624AsnfsTer2
ENST00000614496.4:c.1354dup (MSH6)	ENSP00000477844.1:p.Thr452AsnfsTer2
ENST00000616033.4:c.2257dup (MSH6)	ENSP00000480261.1:p.Thr753AsnfsTer2
ENST00000622629.4:c.-837dup (MSH6)	ENSP00000482078.1:n.-837dup
NM_000179.2:c.2260dup , LRG_219t1:c.2260dup (MSH6)	NP_000170.1:p.Thr754AsnfsTer2
NM_001281492.1:c.1870dup (MSH6)	NP_001268421.1:p.Thr624AsnfsTer2
NM_001281493.1:c.1354dup (MSH6)	NP_001268422.1:p.Thr452AsnfsTer2
NM_001281494.1:c.1354dup (MSH6)	NP_001268423.1:p.Thr452AsnfsTer2
XM_005264271.1:c.1963dup (MSH6)	XP_005264328.1:p.Thr655AsnfsTer2
XM_011532798.1:c.2077dup (MSH6)	XP_011531100.1:p.Thr693AsnfsTer2
XM_011532799.1:c.1963dup (MSH6)	XP_011531101.1:p.Thr655AsnfsTer2
XM_011532800.1:c.1963dup (MSH6)	XP_011531102.1:p.Thr655AsnfsTer2
XM_024452819.1:c.2260dup (MSH6)	XP_024308587.1:p.Thr754AsnfsTer2
XM_024452820.1:c.2077dup (MSH6)	XP_024308588.1:p.Thr693AsnfsTer2
XM_024452821.1:c.1963dup (MSH6)	XP_024308589.1:p.Thr655AsnfsTer2
XM_024452822.1:c.1354dup (MSH6)	XP_024308590.1:p.Thr452AsnfsTer2
NM_000179.3:c.2260dup (MSH6) MANE Select	NP_000170.1:p.Thr754AsnfsTer2
NM_001281492.2:c.1870dup (MSH6)	NP_001268421.1:p.Thr624AsnfsTer2
NM_001281493.2:c.1354dup (MSH6)	NP_001268422.1:p.Thr452AsnfsTer2
NM_001281494.2:c.1354dup (MSH6)	NP_001268423.1:p.Thr452AsnfsTer2