Canonical Allele Identifier: CA2695200588

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 2673582
• ClinVar RCV Id: RCV003450219

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805706_47805710delinsCGTT , CM000664.2:g.47805706_47805710delinsCGTT	GRCh38
NC_000002.11:g.48032845_48032849delinsCGTT , CM000664.1:g.48032845_48032849delinsCGTT	GRCh37
NC_000002.10:g.47886349_47886353delinsCGTT	NCBI36
NG_007111.1:g.27560_27564delinsCGTT , LRG_219:g.27560_27564delinsCGTT
NG_008397.1:g.104966_104970delinsAACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3348_3349+3delinsCGTT (MSH6)
ENST00000420813.6:c.3348_3349+3delinsCGTT (MSH6)
ENST00000455383.6:c.3348_3349+3delinsCGTT (MSH6)
ENST00000700004.2:c.3261_3262+3delinsCGTT (MSH6)
ENST00000699999.1:n.4319_4320+3delinsCGTT (MSH6)
ENST00000700000.1:c.2079_2080+3delinsCGTT (MSH6)
ENST00000700002.1:c.3651_3652+3delinsCGTT (MSH6)
ENST00000700003.1:c.1100_1101+3delinsCGTT (MSH6)
ENST00000700004.1:c.2418_2419+3delinsCGTT (MSH6)
ENST00000700005.1:n.2496_2497+3delinsCGTT (MSH6)
ENST00000700006.1:n.4307_4311delinsCGTT (MSH6)
ENST00000700007.1:n.2240_2241+3delinsCGTT (MSH6)
ENST00000700008.1:n.1814_1815+3delinsCGTT (MSH6)
ENST00000700009.1:n.1813_1817delinsCGTT (MSH6)
ENST00000700010.1:n.1054_1055+3delinsCGTT (MSH6)
ENST00000700011.1:n.2939_2940+3delinsCGTT (MSH6)
ENST00000234420.11:c.3645_3646+3delinsCGTT (MSH6)
ENST00000540021.6:c.3255_3256+3delinsCGTT (MSH6)
ENST00000652107.1:c.3348_3349+3delinsCGTT (MSH6)
ENST00000673637.1:c.3348_3349+3delinsCGTT (MSH6)
ENST00000234420.9:c.3645_3646+3delinsCGTT (MSH6)
ENST00000405808.5:c.169+2485_169+2489delinsAACG (FBXO11)	ENSP00000385127.1:n.169+2485_169+2489delinsAACG
ENST00000434234.5:c.*124+2284_*124+2288delinsAACG (FBXO11)	ENSP00000402692.1:n.*124+2284_*124+2288delinsAACG
ENST00000445503.5:c.*2992_*2993+3delinsCGTT (MSH6)
ENST00000538136.1:c.2739_2740+3delinsCGTT (MSH6)
ENST00000540021.5:c.3255_3256+3delinsCGTT (MSH6)
ENST00000614496.4:c.2739_2740+3delinsCGTT (MSH6)
ENST00000622629.4:c.549_550+3delinsCGTT (MSH6)
NM_000179.2:c.3645_3646+3delinsCGTT , LRG_219t1:c.3645_3646+3delinsCGTT (MSH6)
NM_001281492.1:c.3255_3256+3delinsCGTT (MSH6)
NM_001281493.1:c.2739_2740+3delinsCGTT (MSH6)
NM_001281494.1:c.2739_2740+3delinsCGTT (MSH6)
XM_005264271.1:c.3348_3349+3delinsCGTT (MSH6)
XM_011532798.1:c.3462_3463+3delinsCGTT (MSH6)
XM_011532799.1:c.3348_3349+3delinsCGTT (MSH6)
XM_011532800.1:c.3348_3349+3delinsCGTT (MSH6)
XM_024452819.1:c.3645_3646+3delinsCGTT (MSH6)
XM_024452820.1:c.3462_3463+3delinsCGTT (MSH6)
XM_024452821.1:c.3348_3349+3delinsCGTT (MSH6)
XM_024452822.1:c.2739_2740+3delinsCGTT (MSH6)
NM_000179.3:c.3645_3646+3delinsCGTT (MSH6)
NM_001281492.2:c.3255_3256+3delinsCGTT (MSH6)
NM_001281493.2:c.2739_2740+3delinsCGTT (MSH6)
NM_001281494.2:c.2739_2740+3delinsCGTT (MSH6)