Canonical Allele Identifier: CA658655696

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 485859
• ClinVar RCV Id: RCV000563442
• dbSNP Id: rs1553411441

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47795974_47795976delinsAAC , CM000664.2:g.47795974_47795976delinsAAC	GRCh38
NC_000002.11:g.48023113_48023115delinsAAC , CM000664.1:g.48023113_48023115delinsAAC	GRCh37
NC_000002.10:g.47876617_47876619delinsAAC	NCBI36
NG_007111.1:g.17828_17830delinsAAC , LRG_219:g.17828_17830delinsAAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.241_243delinsAAC (MSH6)	ENSP00000406248.2:p.Asp81Asn
ENST00000420813.6:c.241_243delinsAAC (MSH6)	ENSP00000390382.2:p.Asp81Asn
ENST00000455383.6:c.241_243delinsAAC (MSH6)	ENSP00000397484.2:p.Asp81Asn
ENST00000700004.2:c.538_540delinsAAC (MSH6)	ENSP00000514752.2:p.Asp180Asn
ENST00000699999.1:n.622_624delinsAAC (MSH6)
ENST00000700000.1:c.538_540delinsAAC (MSH6)	ENSP00000514749.1:p.Asp180Asn
ENST00000700001.1:n.610_612delinsAAC (MSH6)
ENST00000700002.1:c.538_540delinsAAC (MSH6)	ENSP00000514750.1:p.Asp180Asn
ENST00000700003.1:c.538_540delinsAAC (MSH6)	ENSP00000514751.1:p.Asp180Asn
ENST00000234420.11:c.538_540delinsAAC (MSH6) MANE Select	ENSP00000234420.5:p.Asp180Asn
ENST00000540021.6:c.238-2637_238-2635delinsAAC (MSH6)	ENSP00000446475.1:n.238-2637_238-2635delinsAAC
ENST00000652107.1:c.241_243delinsAAC (MSH6)	ENSP00000498629.1:p.Asp81Asn
ENST00000673637.1:c.241_243delinsAAC (MSH6)	ENSP00000501310.1:p.Asp81Asn
ENST00000673922.1:n.350-2637_350-2635delinsAAC (MSH6)
ENST00000234420.9:c.538_540delinsAAC (MSH6)	ENSP00000234420.4:p.Asp180Asn
ENST00000405808.5:c.170-6536_170-6534delinsGTT (FBXO11)	ENSP00000385127.1:n.170-6536_170-6534delinsGTT
ENST00000411819.1:c.241_243delinsAAC (MSH6)	ENSP00000406248.1:p.Asp81Asn
ENST00000420813.5:c.241_243delinsAAC (MSH6)	ENSP00000390382.1:p.Asp81Asn
ENST00000434234.5:c.*125-6536_*125-6534delinsGTT (FBXO11)	ENSP00000402692.1:n.*125-6536_*125-6534delinsGTT
ENST00000445503.5:c.458-2637_458-2635delinsAAC (MSH6)	ENSP00000405294.1:n.458-2637_458-2635delinsAAC
ENST00000455383.5:c.241_243delinsAAC (MSH6)	ENSP00000397484.1:p.Asp81Asn
ENST00000456246.1:c.*26_*28delinsAAC (MSH6)	ENSP00000410570.1:n.*26_*28delinsAAC
ENST00000538136.1:c.-365_-363delinsAAC (MSH6)	ENSP00000438580.1:n.-365_-363delinsAAC
ENST00000540021.5:c.238-2637_238-2635delinsAAC (MSH6)	ENSP00000446475.1:n.238-2637_238-2635delinsAAC
ENST00000614496.4:c.-279-2637_-279-2635delinsAAC (MSH6)	ENSP00000477844.1:n.-279-2637_-279-2635delinsAAC
ENST00000616033.4:c.535_537delinsAAC (MSH6)	ENSP00000480261.1:p.Asp179Asn
ENST00000622629.4:c.-2559_-2557delinsAAC (MSH6)	ENSP00000482078.1:n.-2559_-2557delinsAAC
NM_000179.2:c.538_540delinsAAC , LRG_219t1:c.538_540delinsAAC (MSH6)	NP_000170.1:p.Asp180Asn
NM_001281492.1:c.238-2637_238-2635delinsAAC (MSH6)	NP_001268421.1:n.238-2637_238-2635delinsAAC
NM_001281493.1:c.-279-2637_-279-2635delinsAAC (MSH6)	NP_001268422.1:n.-279-2637_-279-2635delinsAAC
NM_001281494.1:c.-365_-363delinsAAC (MSH6)	NP_001268423.1:n.-365_-363delinsAAC
XM_005264271.1:c.241_243delinsAAC (MSH6)	XP_005264328.1:p.Asp81Asn
XM_011532798.1:c.355_357delinsAAC (MSH6)	XP_011531100.1:p.Asp119Asn
XM_011532799.1:c.241_243delinsAAC (MSH6)	XP_011531101.1:p.Asp81Asn
XM_011532800.1:c.241_243delinsAAC (MSH6)	XP_011531102.1:p.Asp81Asn
XM_024452819.1:c.538_540delinsAAC (MSH6)	XP_024308587.1:p.Asp180Asn
XM_024452820.1:c.355_357delinsAAC (MSH6)	XP_024308588.1:p.Asp119Asn
XM_024452821.1:c.241_243delinsAAC (MSH6)	XP_024308589.1:p.Asp81Asn
XM_024452822.1:c.-279-2637_-279-2635delinsAAC (MSH6)	XP_024308590.1:n.-279-2637_-279-2635delinsAAC
NM_000179.3:c.538_540delinsAAC (MSH6) MANE Select	NP_000170.1:p.Asp180Asn
NM_001281492.2:c.238-2637_238-2635delinsAAC (MSH6)	NP_001268421.1:n.238-2637_238-2635delinsAAC
NM_001281493.2:c.-279-2637_-279-2635delinsAAC (MSH6)	NP_001268422.1:n.-279-2637_-279-2635delinsAAC
NM_001281494.2:c.-365_-363delinsAAC (MSH6)	NP_001268423.1:n.-365_-363delinsAAC