Canonical Allele Identifier: CA2838032275

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799116_47799118delinsAAC , CM000664.2:g.47799116_47799118delinsAAC	GRCh38
NC_000002.11:g.48026255_48026257delinsAAC , CM000664.1:g.48026255_48026257delinsAAC	GRCh37
NC_000002.10:g.47879759_47879761delinsAAC	NCBI36
NG_007111.1:g.20970_20972delinsAAC , LRG_219:g.20970_20972delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.836_838delinsAAC (MSH6)	ENSP00000406248.2:p.Arg279Lys
ENST00000420813.6:c.836_838delinsAAC (MSH6)	ENSP00000390382.2:p.Arg279Lys
ENST00000455383.6:c.836_838delinsAAC (MSH6)	ENSP00000397484.2:p.Arg279Lys
ENST00000700004.2:c.1133_1135delinsAAC (MSH6)	ENSP00000514752.2:p.Arg378Lys
ENST00000699999.1:n.1217_1219delinsAAC (MSH6)
ENST00000700000.1:c.1133_1135delinsAAC (MSH6)	ENSP00000514749.1:p.Arg378Lys
ENST00000700002.1:c.1139_1141delinsAAC (MSH6)	ENSP00000514750.1:p.Arg380Lys
ENST00000700003.1:c.627+3053_627+3055delinsAAC (MSH6)	ENSP00000514751.1:n.627+3053_627+3055delinsAAC
ENST00000700004.1:c.290_292delinsAAC (MSH6)	ENSP00000514752.1:p.Arg97Lys
ENST00000234420.11:c.1133_1135delinsAAC (MSH6) MANE Select	ENSP00000234420.5:p.Arg378Lys
ENST00000540021.6:c.743_745delinsAAC (MSH6)	ENSP00000446475.1:p.Arg248Lys
ENST00000652107.1:c.836_838delinsAAC (MSH6)	ENSP00000498629.1:p.Arg279Lys
ENST00000673637.1:c.836_838delinsAAC (MSH6)	ENSP00000501310.1:p.Arg279Lys
ENST00000234420.9:c.1133_1135delinsAAC (MSH6)	ENSP00000234420.4:p.Arg378Lys
ENST00000405808.5:c.169+9077_169+9079delinsGTT (FBXO11)	ENSP00000385127.1:n.169+9077_169+9079delinsGTT
ENST00000434234.5:c.*124+8876_*124+8878delinsGTT (FBXO11)	ENSP00000402692.1:n.*124+8876_*124+8878delinsGTT
ENST00000445503.5:c.*480_*482delinsAAC (MSH6)	ENSP00000405294.1:n.*480_*482delinsAAC
ENST00000538136.1:c.227_229delinsAAC (MSH6)	ENSP00000438580.1:p.Arg76Lys
ENST00000540021.5:c.743_745delinsAAC (MSH6)	ENSP00000446475.1:p.Arg248Lys
ENST00000614496.4:c.227_229delinsAAC (MSH6)	ENSP00000477844.1:p.Arg76Lys
ENST00000616033.4:c.1130_1132delinsAAC (MSH6)	ENSP00000480261.1:p.Arg377Lys
ENST00000622629.4:c.-1964_-1962delinsAAC (MSH6)	ENSP00000482078.1:n.-1964_-1962delinsAAC
NM_000179.2:c.1133_1135delinsAAC , LRG_219t1:c.1133_1135delinsAAC (MSH6)	NP_000170.1:p.Arg378Lys
NM_001281492.1:c.743_745delinsAAC (MSH6)	NP_001268421.1:p.Arg248Lys
NM_001281493.1:c.227_229delinsAAC (MSH6)	NP_001268422.1:p.Arg76Lys
NM_001281494.1:c.227_229delinsAAC (MSH6)	NP_001268423.1:p.Arg76Lys
XM_005264271.1:c.836_838delinsAAC (MSH6)	XP_005264328.1:p.Arg279Lys
XM_011532798.1:c.950_952delinsAAC (MSH6)	XP_011531100.1:p.Arg317Lys
XM_011532799.1:c.836_838delinsAAC (MSH6)	XP_011531101.1:p.Arg279Lys
XM_011532800.1:c.836_838delinsAAC (MSH6)	XP_011531102.1:p.Arg279Lys
XM_024452819.1:c.1133_1135delinsAAC (MSH6)	XP_024308587.1:p.Arg378Lys
XM_024452820.1:c.950_952delinsAAC (MSH6)	XP_024308588.1:p.Arg317Lys
XM_024452821.1:c.836_838delinsAAC (MSH6)	XP_024308589.1:p.Arg279Lys
XM_024452822.1:c.227_229delinsAAC (MSH6)	XP_024308590.1:p.Arg76Lys
NM_000179.3:c.1133_1135delinsAAC (MSH6) MANE Select	NP_000170.1:p.Arg378Lys
NM_001281492.2:c.743_745delinsAAC (MSH6)	NP_001268421.1:p.Arg248Lys
NM_001281493.2:c.227_229delinsAAC (MSH6)	NP_001268422.1:p.Arg76Lys
NM_001281494.2:c.227_229delinsAAC (MSH6)	NP_001268423.1:p.Arg76Lys