Canonical Allele Identifier: CA2658948825

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47796172-ATTATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47796178_47796182del , CM000664.2:g.47796178_47796182del	GRCh38
NC_000002.11:g.48023317_48023321del , CM000664.1:g.48023317_48023321del	GRCh37
NC_000002.10:g.47876821_47876825del	NCBI36
NG_007111.1:g.18032_18036del , LRG_219:g.18032_18036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.330+115_330+119del (MSH6)	ENSP00000406248.2:n.330+115_330+119del
ENST00000420813.6:c.330+115_330+119del (MSH6)	ENSP00000390382.2:n.330+115_330+119del
ENST00000455383.6:c.330+115_330+119del (MSH6)	ENSP00000397484.2:n.330+115_330+119del
ENST00000700004.2:c.627+115_627+119del (MSH6)	ENSP00000514752.2:n.627+115_627+119del
ENST00000699999.1:n.711+115_711+119del (MSH6)
ENST00000700000.1:c.627+115_627+119del (MSH6)	ENSP00000514749.1:n.627+115_627+119del
ENST00000700001.1:n.814_818del (MSH6)
ENST00000700002.1:c.637+105_637+109del (MSH6)	ENSP00000514750.1:n.637+105_637+109del
ENST00000700003.1:c.627+115_627+119del (MSH6)	ENSP00000514751.1:n.627+115_627+119del
ENST00000234420.11:c.627+115_627+119del (MSH6) MANE Select	ENSP00000234420.5:n.627+115_627+119del
ENST00000540021.6:c.238-2433_238-2429del (MSH6)	ENSP00000446475.1:n.238-2433_238-2429del
ENST00000652107.1:c.330+115_330+119del (MSH6)	ENSP00000498629.1:n.330+115_330+119del
ENST00000673637.1:c.330+115_330+119del (MSH6)	ENSP00000501310.1:n.330+115_330+119del
ENST00000673922.1:n.350-2433_350-2429del (MSH6)
ENST00000234420.9:c.627+115_627+119del (MSH6)	ENSP00000234420.4:n.627+115_627+119del
ENST00000405808.5:c.170-6737_170-6733del (FBXO11)	ENSP00000385127.1:n.170-6737_170-6733del
ENST00000411819.1:c.330+115_330+119del (MSH6)	ENSP00000406248.1:n.330+115_330+119del
ENST00000434234.5:c.*125-6737_*125-6733del (FBXO11)	ENSP00000402692.1:n.*125-6737_*125-6733del
ENST00000445503.5:c.458-2433_458-2429del (MSH6)	ENSP00000405294.1:n.458-2433_458-2429del
ENST00000455383.5:c.330+115_330+119del (MSH6)	ENSP00000397484.1:n.330+115_330+119del
ENST00000456246.1:c.*115+115_*115+119del (MSH6)	ENSP00000410570.1:n.*115+115_*115+119del
ENST00000538136.1:c.-276+115_-276+119del (MSH6)	ENSP00000438580.1:n.-276+115_-276+119del
ENST00000540021.5:c.238-2433_238-2429del (MSH6)	ENSP00000446475.1:n.238-2433_238-2429del
ENST00000614496.4:c.-279-2433_-279-2429del (MSH6)	ENSP00000477844.1:n.-279-2433_-279-2429del
ENST00000616033.4:c.624+115_624+119del (MSH6)	ENSP00000480261.1:n.624+115_624+119del
ENST00000622629.4:c.-2470+115_-2470+119del (MSH6)	ENSP00000482078.1:n.-2470+115_-2470+119del
NM_000179.2:c.627+115_627+119del , LRG_219t1:c.627+115_627+119del (MSH6)	NP_000170.1:n.627+115_627+119del
NM_001281492.1:c.238-2433_238-2429del (MSH6)	NP_001268421.1:n.238-2433_238-2429del
NM_001281493.1:c.-279-2433_-279-2429del (MSH6)	NP_001268422.1:n.-279-2433_-279-2429del
NM_001281494.1:c.-276+115_-276+119del (MSH6)	NP_001268423.1:n.-276+115_-276+119del
XM_005264271.1:c.330+115_330+119del (MSH6)	XP_005264328.1:n.330+115_330+119del
XM_011532798.1:c.444+115_444+119del (MSH6)	XP_011531100.1:n.444+115_444+119del
XM_011532799.1:c.330+115_330+119del (MSH6)	XP_011531101.1:n.330+115_330+119del
XM_011532800.1:c.330+115_330+119del (MSH6)	XP_011531102.1:n.330+115_330+119del
XM_024452819.1:c.627+115_627+119del (MSH6)	XP_024308587.1:n.627+115_627+119del
XM_024452820.1:c.444+115_444+119del (MSH6)	XP_024308588.1:n.444+115_444+119del
XM_024452821.1:c.330+115_330+119del (MSH6)	XP_024308589.1:n.330+115_330+119del
XM_024452822.1:c.-279-2433_-279-2429del (MSH6)	XP_024308590.1:n.-279-2433_-279-2429del
NM_000179.3:c.627+115_627+119del (MSH6) MANE Select	NP_000170.1:n.627+115_627+119del
NM_001281492.2:c.238-2433_238-2429del (MSH6)	NP_001268421.1:n.238-2433_238-2429del
NM_001281493.2:c.-279-2433_-279-2429del (MSH6)	NP_001268422.1:n.-279-2433_-279-2429del
NM_001281494.2:c.-276+115_-276+119del (MSH6)	NP_001268423.1:n.-276+115_-276+119del