Canonical Allele Identifier: CA2658948822

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47796170-GTAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47796175_47796177del , CM000664.2:g.47796175_47796177del	GRCh38
NC_000002.11:g.48023314_48023316del , CM000664.1:g.48023314_48023316del	GRCh37
NC_000002.10:g.47876818_47876820del	NCBI36
NG_007111.1:g.18029_18031del , LRG_219:g.18029_18031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.330+112_330+114del (MSH6)	ENSP00000406248.2:n.330+112_330+114del
ENST00000420813.6:c.330+112_330+114del (MSH6)	ENSP00000390382.2:n.330+112_330+114del
ENST00000455383.6:c.330+112_330+114del (MSH6)	ENSP00000397484.2:n.330+112_330+114del
ENST00000700004.2:c.627+112_627+114del (MSH6)	ENSP00000514752.2:n.627+112_627+114del
ENST00000699999.1:n.711+112_711+114del (MSH6)
ENST00000700000.1:c.627+112_627+114del (MSH6)	ENSP00000514749.1:n.627+112_627+114del
ENST00000700001.1:n.811_813del (MSH6)
ENST00000700002.1:c.637+102_637+104del (MSH6)	ENSP00000514750.1:n.637+102_637+104del
ENST00000700003.1:c.627+112_627+114del (MSH6)	ENSP00000514751.1:n.627+112_627+114del
ENST00000234420.11:c.627+112_627+114del (MSH6) MANE Select	ENSP00000234420.5:n.627+112_627+114del
ENST00000540021.6:c.238-2436_238-2434del (MSH6)	ENSP00000446475.1:n.238-2436_238-2434del
ENST00000652107.1:c.330+112_330+114del (MSH6)	ENSP00000498629.1:n.330+112_330+114del
ENST00000673637.1:c.330+112_330+114del (MSH6)	ENSP00000501310.1:n.330+112_330+114del
ENST00000673922.1:n.350-2436_350-2434del (MSH6)
ENST00000234420.9:c.627+112_627+114del (MSH6)	ENSP00000234420.4:n.627+112_627+114del
ENST00000405808.5:c.170-6733_170-6731del (FBXO11)	ENSP00000385127.1:n.170-6733_170-6731del
ENST00000411819.1:c.330+112_330+114del (MSH6)	ENSP00000406248.1:n.330+112_330+114del
ENST00000434234.5:c.*125-6733_*125-6731del (FBXO11)	ENSP00000402692.1:n.*125-6733_*125-6731del
ENST00000445503.5:c.458-2436_458-2434del (MSH6)	ENSP00000405294.1:n.458-2436_458-2434del
ENST00000455383.5:c.330+112_330+114del (MSH6)	ENSP00000397484.1:n.330+112_330+114del
ENST00000456246.1:c.*115+112_*115+114del (MSH6)	ENSP00000410570.1:n.*115+112_*115+114del
ENST00000538136.1:c.-276+112_-276+114del (MSH6)	ENSP00000438580.1:n.-276+112_-276+114del
ENST00000540021.5:c.238-2436_238-2434del (MSH6)	ENSP00000446475.1:n.238-2436_238-2434del
ENST00000614496.4:c.-279-2436_-279-2434del (MSH6)	ENSP00000477844.1:n.-279-2436_-279-2434del
ENST00000616033.4:c.624+112_624+114del (MSH6)	ENSP00000480261.1:n.624+112_624+114del
ENST00000622629.4:c.-2470+112_-2470+114del (MSH6)	ENSP00000482078.1:n.-2470+112_-2470+114del
NM_000179.2:c.627+112_627+114del , LRG_219t1:c.627+112_627+114del (MSH6)	NP_000170.1:n.627+112_627+114del
NM_001281492.1:c.238-2436_238-2434del (MSH6)	NP_001268421.1:n.238-2436_238-2434del
NM_001281493.1:c.-279-2436_-279-2434del (MSH6)	NP_001268422.1:n.-279-2436_-279-2434del
NM_001281494.1:c.-276+112_-276+114del (MSH6)	NP_001268423.1:n.-276+112_-276+114del
XM_005264271.1:c.330+112_330+114del (MSH6)	XP_005264328.1:n.330+112_330+114del
XM_011532798.1:c.444+112_444+114del (MSH6)	XP_011531100.1:n.444+112_444+114del
XM_011532799.1:c.330+112_330+114del (MSH6)	XP_011531101.1:n.330+112_330+114del
XM_011532800.1:c.330+112_330+114del (MSH6)	XP_011531102.1:n.330+112_330+114del
XM_024452819.1:c.627+112_627+114del (MSH6)	XP_024308587.1:n.627+112_627+114del
XM_024452820.1:c.444+112_444+114del (MSH6)	XP_024308588.1:n.444+112_444+114del
XM_024452821.1:c.330+112_330+114del (MSH6)	XP_024308589.1:n.330+112_330+114del
XM_024452822.1:c.-279-2436_-279-2434del (MSH6)	XP_024308590.1:n.-279-2436_-279-2434del
NM_000179.3:c.627+112_627+114del (MSH6) MANE Select	NP_000170.1:n.627+112_627+114del
NM_001281492.2:c.238-2436_238-2434del (MSH6)	NP_001268421.1:n.238-2436_238-2434del
NM_001281493.2:c.-279-2436_-279-2434del (MSH6)	NP_001268422.1:n.-279-2436_-279-2434del
NM_001281494.2:c.-276+112_-276+114del (MSH6)	NP_001268423.1:n.-276+112_-276+114del