Canonical Allele Identifier: CA10577268

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 234761
• ClinVar RCV Id: RCV000215322 ; RCV000491140 ; RCV000557139 ; RCV003454678 ; RCV003463618
• dbSNP Id: rs876661205
• gnomAD v4: 2-47799948-AC-A
• MyVariant Identifiers: chr2:g.48027091del (hg19) ; chr2:g.47799952del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799952del , CM000664.2:g.47799952del	GRCh38
NC_000002.11:g.48027091del , CM000664.1:g.48027091del	GRCh37
NC_000002.10:g.47880595del	NCBI36
NG_007111.1:g.21806del , LRG_219:g.21806del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1672del (MSH6)	ENSP00000406248.2:p.Gln558ArgfsTer6
ENST00000420813.6:c.1672del (MSH6)	ENSP00000390382.2:p.Gln558ArgfsTer6
ENST00000455383.6:c.1672del (MSH6)	ENSP00000397484.2:p.Gln558ArgfsTer6
ENST00000700004.2:c.1969del (MSH6)	ENSP00000514752.2:p.Gln657ArgfsTer6
ENST00000699999.1:n.2053del (MSH6)
ENST00000700000.1:c.1606+363del (MSH6)	ENSP00000514749.1:n.1606+363del
ENST00000700002.1:c.1975del (MSH6)	ENSP00000514750.1:p.Gln659ArgfsTer6
ENST00000700003.1:c.628-3468del (MSH6)	ENSP00000514751.1:n.628-3468del
ENST00000700004.1:c.1126del (MSH6)	ENSP00000514752.1:p.Gln376ArgfsTer6
ENST00000234420.11:c.1969del (MSH6) MANE Select	ENSP00000234420.5:p.Gln657ArgfsTer6
ENST00000540021.6:c.1579del (MSH6)	ENSP00000446475.1:p.Gln527ArgfsTer6
ENST00000652107.1:c.1672del (MSH6)	ENSP00000498629.1:p.Gln558ArgfsTer6
ENST00000673637.1:c.1672del (MSH6)	ENSP00000501310.1:p.Gln558ArgfsTer6
ENST00000234420.9:c.1969del (MSH6)	ENSP00000234420.4:p.Gln657ArgfsTer6
ENST00000405808.5:c.169+8246del (FBXO11)	ENSP00000385127.1:n.169+8246del
ENST00000434234.5:c.*124+8045del (FBXO11)	ENSP00000402692.1:n.*124+8045del
ENST00000445503.5:c.*1316del (MSH6)	ENSP00000405294.1:n.*1316del
ENST00000538136.1:c.1063del (MSH6)	ENSP00000438580.1:p.Gln355ArgfsTer6
ENST00000540021.5:c.1579del (MSH6)	ENSP00000446475.1:p.Gln527ArgfsTer6
ENST00000614496.4:c.1063del (MSH6)	ENSP00000477844.1:p.Gln355ArgfsTer6
ENST00000616033.4:c.1966del (MSH6)	ENSP00000480261.1:p.Gln656ArgfsTer6
ENST00000622629.4:c.-1128del (MSH6)	ENSP00000482078.1:n.-1128del
NM_000179.2:c.1969del , LRG_219t1:c.1969del (MSH6)	NP_000170.1:p.Gln657ArgfsTer6
NM_001281492.1:c.1579del (MSH6)	NP_001268421.1:p.Gln527ArgfsTer6
NM_001281493.1:c.1063del (MSH6)	NP_001268422.1:p.Gln355ArgfsTer6
NM_001281494.1:c.1063del (MSH6)	NP_001268423.1:p.Gln355ArgfsTer6
XM_005264271.1:c.1672del (MSH6)	XP_005264328.1:p.Gln558ArgfsTer6
XM_011532798.1:c.1786del (MSH6)	XP_011531100.1:p.Gln596ArgfsTer6
XM_011532799.1:c.1672del (MSH6)	XP_011531101.1:p.Gln558ArgfsTer6
XM_011532800.1:c.1672del (MSH6)	XP_011531102.1:p.Gln558ArgfsTer6
XM_024452819.1:c.1969del (MSH6)	XP_024308587.1:p.Gln657ArgfsTer6
XM_024452820.1:c.1786del (MSH6)	XP_024308588.1:p.Gln596ArgfsTer6
XM_024452821.1:c.1672del (MSH6)	XP_024308589.1:p.Gln558ArgfsTer6
XM_024452822.1:c.1063del (MSH6)	XP_024308590.1:p.Gln355ArgfsTer6
NM_000179.3:c.1969del (MSH6) MANE Select	NP_000170.1:p.Gln657ArgfsTer6
NM_001281492.2:c.1579del (MSH6)	NP_001268421.1:p.Gln527ArgfsTer6
NM_001281493.2:c.1063del (MSH6)	NP_001268422.1:p.Gln355ArgfsTer6
NM_001281494.2:c.1063del (MSH6)	NP_001268423.1:p.Gln355ArgfsTer6