Canonical Allele Identifier: CA645514866

Gene: MSH6 FBXO11

Linked Data

• COSMIC: COSM5967514

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798913dup , CM000664.2:g.47798913dup	GRCh38
NC_000002.11:g.48026052dup , CM000664.1:g.48026052dup	GRCh37
NC_000002.10:g.47879556dup	NCBI36
NG_007111.1:g.20767dup , LRG_219:g.20767dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.633dup (MSH6)	ENSP00000406248.2:p.Lys212Ter
ENST00000420813.6:c.633dup (MSH6)	ENSP00000390382.2:p.Lys212Ter
ENST00000455383.6:c.633dup (MSH6)	ENSP00000397484.2:p.Lys212Ter
ENST00000700004.2:c.930dup (MSH6)	ENSP00000514752.2:p.Lys311Ter
ENST00000699999.1:n.1014dup (MSH6)
ENST00000700000.1:c.930dup (MSH6)	ENSP00000514749.1:p.Lys311Ter
ENST00000700002.1:c.936dup (MSH6)	ENSP00000514750.1:p.Lys313Ter
ENST00000700003.1:c.627+2850dup (MSH6)	ENSP00000514751.1:n.627+2850dup
ENST00000700004.1:c.87dup (MSH6)	ENSP00000514752.1:p.Lys30Ter
ENST00000234420.11:c.930dup (MSH6) MANE Select	ENSP00000234420.5:p.Lys311Ter
ENST00000540021.6:c.540dup (MSH6)	ENSP00000446475.1:p.Lys181Ter
ENST00000652107.1:c.633dup (MSH6)	ENSP00000498629.1:p.Lys212Ter
ENST00000673637.1:c.633dup (MSH6)	ENSP00000501310.1:p.Lys212Ter
ENST00000234420.9:c.930dup (MSH6)	ENSP00000234420.4:p.Lys311Ter
ENST00000405808.5:c.169+9283dup (FBXO11)	ENSP00000385127.1:n.169+9283dup
ENST00000434234.5:c.*124+9082dup (FBXO11)	ENSP00000402692.1:n.*124+9082dup
ENST00000445503.5:c.*277dup (MSH6)	ENSP00000405294.1:n.*277dup
ENST00000456246.1:c.*418dup (MSH6)	ENSP00000410570.1:n.*418dup
ENST00000538136.1:c.24dup (MSH6)	ENSP00000438580.1:p.Lys9Ter
ENST00000540021.5:c.540dup (MSH6)	ENSP00000446475.1:p.Lys181Ter
ENST00000614496.4:c.24dup (MSH6)	ENSP00000477844.1:p.Lys9Ter
ENST00000616033.4:c.927dup (MSH6)	ENSP00000480261.1:p.Lys310Ter
ENST00000622629.4:c.-2167dup (MSH6)	ENSP00000482078.1:n.-2167dup
NM_000179.2:c.930dup , LRG_219t1:c.930dup (MSH6)	NP_000170.1:p.Lys311Ter
NM_001281492.1:c.540dup (MSH6)	NP_001268421.1:p.Lys181Ter
NM_001281493.1:c.24dup (MSH6)	NP_001268422.1:p.Lys9Ter
NM_001281494.1:c.24dup (MSH6)	NP_001268423.1:p.Lys9Ter
XM_005264271.1:c.633dup (MSH6)	XP_005264328.1:p.Lys212Ter
XM_011532798.1:c.747dup (MSH6)	XP_011531100.1:p.Lys250Ter
XM_011532799.1:c.633dup (MSH6)	XP_011531101.1:p.Lys212Ter
XM_011532800.1:c.633dup (MSH6)	XP_011531102.1:p.Lys212Ter
XM_024452819.1:c.930dup (MSH6)	XP_024308587.1:p.Lys311Ter
XM_024452820.1:c.747dup (MSH6)	XP_024308588.1:p.Lys250Ter
XM_024452821.1:c.633dup (MSH6)	XP_024308589.1:p.Lys212Ter
XM_024452822.1:c.24dup (MSH6)	XP_024308590.1:p.Lys9Ter
NM_000179.3:c.930dup (MSH6) MANE Select	NP_000170.1:p.Lys311Ter
NM_001281492.2:c.540dup (MSH6)	NP_001268421.1:p.Lys181Ter
NM_001281493.2:c.24dup (MSH6)	NP_001268422.1:p.Lys9Ter
NM_001281494.2:c.24dup (MSH6)	NP_001268423.1:p.Lys9Ter