Canonical Allele Identifier: CA2496053707

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1669999256

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805889_47805892dup , CM000664.2:g.47805889_47805892dup	GRCh38
NC_000002.11:g.48033028_48033031dup , CM000664.1:g.48033028_48033031dup	GRCh37
NC_000002.10:g.47886532_47886535dup	NCBI36
NG_007111.1:g.27743_27746dup , LRG_219:g.27743_27746dup
NG_008397.1:g.104786_104789dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3349+182_3349+185dup (MSH6)	ENSP00000406248.2:n.3349+182_3349+185dup
ENST00000420813.6:c.3349+182_3349+185dup (MSH6)	ENSP00000390382.2:n.3349+182_3349+185dup
ENST00000455383.6:c.3349+182_3349+185dup (MSH6)	ENSP00000397484.2:n.3349+182_3349+185dup
ENST00000700004.2:c.3262+182_3262+185dup (MSH6)	ENSP00000514752.2:n.3262+182_3262+185dup
ENST00000699999.1:n.4320+182_4320+185dup (MSH6)
ENST00000700000.1:c.2080+182_2080+185dup (MSH6)	ENSP00000514749.1:n.2080+182_2080+185dup
ENST00000700002.1:c.3652+182_3652+185dup (MSH6)	ENSP00000514750.1:n.3652+182_3652+185dup
ENST00000700003.1:c.1101+182_1101+185dup (MSH6)	ENSP00000514751.1:n.1101+182_1101+185dup
ENST00000700004.1:c.2419+182_2419+185dup (MSH6)	ENSP00000514752.1:n.2419+182_2419+185dup
ENST00000700005.1:n.2497+182_2497+185dup (MSH6)
ENST00000700006.1:n.4490_4493dup (MSH6)
ENST00000700007.1:n.2241+182_2241+185dup (MSH6)
ENST00000700008.1:n.1815+182_1815+185dup (MSH6)
ENST00000700009.1:n.1996_1999dup (MSH6)
ENST00000700010.1:n.1055+182_1055+185dup (MSH6)
ENST00000700011.1:n.2940+182_2940+185dup (MSH6)
ENST00000234420.11:c.3646+182_3646+185dup (MSH6) MANE Select	ENSP00000234420.5:n.3646+182_3646+185dup
ENST00000540021.6:c.3256+182_3256+185dup (MSH6)	ENSP00000446475.1:n.3256+182_3256+185dup
ENST00000652107.1:c.3349+182_3349+185dup (MSH6)	ENSP00000498629.1:n.3349+182_3349+185dup
ENST00000673637.1:c.3349+182_3349+185dup (MSH6)	ENSP00000501310.1:n.3349+182_3349+185dup
ENST00000234420.9:c.3646+182_3646+185dup (MSH6)	ENSP00000234420.4:n.3646+182_3646+185dup
ENST00000405808.5:c.169+2305_169+2308dup (FBXO11)	ENSP00000385127.1:n.169+2305_169+2308dup
ENST00000434234.5:c.*124+2104_*124+2107dup (FBXO11)	ENSP00000402692.1:n.*124+2104_*124+2107dup
ENST00000445503.5:c.*2993+182_*2993+185dup (MSH6)	ENSP00000405294.1:n.*2993+182_*2993+185dup
ENST00000538136.1:c.2740+182_2740+185dup (MSH6)	ENSP00000438580.1:n.2740+182_2740+185dup
ENST00000540021.5:c.3256+182_3256+185dup (MSH6)	ENSP00000446475.1:n.3256+182_3256+185dup
ENST00000614496.4:c.2740+182_2740+185dup (MSH6)	ENSP00000477844.1:n.2740+182_2740+185dup
ENST00000622629.4:c.550+182_550+185dup (MSH6)	ENSP00000482078.1:n.550+182_550+185dup
NM_000179.2:c.3646+182_3646+185dup , LRG_219t1:c.3646+182_3646+185dup (MSH6)	NP_000170.1:n.3646+182_3646+185dup
NM_001281492.1:c.3256+182_3256+185dup (MSH6)	NP_001268421.1:n.3256+182_3256+185dup
NM_001281493.1:c.2740+182_2740+185dup (MSH6)	NP_001268422.1:n.2740+182_2740+185dup
NM_001281494.1:c.2740+182_2740+185dup (MSH6)	NP_001268423.1:n.2740+182_2740+185dup
XM_005264271.1:c.3349+182_3349+185dup (MSH6)	XP_005264328.1:n.3349+182_3349+185dup
XM_011532798.1:c.3463+182_3463+185dup (MSH6)	XP_011531100.1:n.3463+182_3463+185dup
XM_011532799.1:c.3349+182_3349+185dup (MSH6)	XP_011531101.1:n.3349+182_3349+185dup
XM_011532800.1:c.3349+182_3349+185dup (MSH6)	XP_011531102.1:n.3349+182_3349+185dup
XM_024452819.1:c.3646+182_3646+185dup (MSH6)	XP_024308587.1:n.3646+182_3646+185dup
XM_024452820.1:c.3463+182_3463+185dup (MSH6)	XP_024308588.1:n.3463+182_3463+185dup
XM_024452821.1:c.3349+182_3349+185dup (MSH6)	XP_024308589.1:n.3349+182_3349+185dup
XM_024452822.1:c.2740+182_2740+185dup (MSH6)	XP_024308590.1:n.2740+182_2740+185dup
NM_000179.3:c.3646+182_3646+185dup (MSH6) MANE Select	NP_000170.1:n.3646+182_3646+185dup
NM_001281492.2:c.3256+182_3256+185dup (MSH6)	NP_001268421.1:n.3256+182_3256+185dup
NM_001281493.2:c.2740+182_2740+185dup (MSH6)	NP_001268422.1:n.2740+182_2740+185dup
NM_001281494.2:c.2740+182_2740+185dup (MSH6)	NP_001268423.1:n.2740+182_2740+185dup