Canonical Allele Identifier: CA2586964959

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804998_47805020del , CM000664.2:g.47804998_47805020del	GRCh38
NC_000002.11:g.48032137_48032159del , CM000664.1:g.48032137_48032159del	GRCh37
NC_000002.10:g.47885641_47885663del	NCBI36
NG_007111.1:g.26852_26874del , LRG_219:g.26852_26874del
NG_008397.1:g.105658_105680del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3230_3252del (MSH6)	ENSP00000406248.2:p.Arg1077AsnfsTer4
ENST00000420813.6:c.3230_3252del (MSH6)	ENSP00000390382.2:p.Arg1077AsnfsTer4
ENST00000455383.6:c.3230_3252del (MSH6)	ENSP00000397484.2:p.Arg1077AsnfsTer4
ENST00000700004.2:c.3173-620_3173-598del (MSH6)	ENSP00000514752.2:n.3173-620_3173-598del
ENST00000699999.1:n.3611_3633del (MSH6)
ENST00000700000.1:c.1961_1983del (MSH6)	ENSP00000514749.1:p.Arg654AsnfsTer4
ENST00000700002.1:c.3533_3555del (MSH6)	ENSP00000514750.1:p.Arg1178AsnfsTer4
ENST00000700003.1:c.982_1004del (MSH6)	ENSP00000514751.1:n.982_1004del
ENST00000700004.1:c.2330-620_2330-598del (MSH6)	ENSP00000514752.1:n.2330-620_2330-598del
ENST00000700005.1:n.2378_2400del (MSH6)
ENST00000700006.1:n.3599_3621del (MSH6)
ENST00000700007.1:n.1532_1554del (MSH6)
ENST00000700008.1:n.1106_1128del (MSH6)
ENST00000700009.1:n.1105_1127del (MSH6)
ENST00000700010.1:n.936_958del (MSH6)
ENST00000700011.1:n.2231_2253del (MSH6)
ENST00000234420.11:c.3527_3549del (MSH6) MANE Select	ENSP00000234420.5:p.Arg1176AsnfsTer4
ENST00000540021.6:c.3137_3159del (MSH6)	ENSP00000446475.1:p.Arg1046AsnfsTer4
ENST00000652107.1:c.3230_3252del (MSH6)	ENSP00000498629.1:p.Arg1077AsnfsTer4
ENST00000673637.1:c.3230_3252del (MSH6)	ENSP00000501310.1:p.Arg1077AsnfsTer4
ENST00000234420.9:c.3527_3549del (MSH6)	ENSP00000234420.4:p.Arg1176AsnfsTer4
ENST00000405808.5:c.169+3177_169+3199del (FBXO11)	ENSP00000385127.1:n.169+3177_169+3199del
ENST00000434234.5:c.*124+2976_*124+2998del (FBXO11)	ENSP00000402692.1:n.*124+2976_*124+2998de...
ENST00000445503.5:c.*2874_*2896del (MSH6)	ENSP00000405294.1:n.*2874_*2896del
ENST00000538136.1:c.2621_2643del (MSH6)	ENSP00000438580.1:p.Arg874AsnfsTer4
ENST00000540021.5:c.3137_3159del (MSH6)	ENSP00000446475.1:p.Arg1046AsnfsTer4
ENST00000614496.4:c.2621_2643del (MSH6)	ENSP00000477844.1:p.Arg874AsnfsTer4
ENST00000622629.4:c.431_453del (MSH6)	ENSP00000482078.1:p.Arg144AsnfsTer4
NM_000179.2:c.3527_3549del , LRG_219t1:c.3527_3549del (MSH6)	NP_000170.1:p.Arg1176AsnfsTer4
NM_001281492.1:c.3137_3159del (MSH6)	NP_001268421.1:p.Arg1046AsnfsTer4
NM_001281493.1:c.2621_2643del (MSH6)	NP_001268422.1:p.Arg874AsnfsTer4
NM_001281494.1:c.2621_2643del (MSH6)	NP_001268423.1:p.Arg874AsnfsTer4
XM_005264271.1:c.3230_3252del (MSH6)	XP_005264328.1:p.Arg1077AsnfsTer4
XM_011532798.1:c.3344_3366del (MSH6)	XP_011531100.1:p.Arg1115AsnfsTer4
XM_011532799.1:c.3230_3252del (MSH6)	XP_011531101.1:p.Arg1077AsnfsTer4
XM_011532800.1:c.3230_3252del (MSH6)	XP_011531102.1:p.Arg1077AsnfsTer4
XM_024452819.1:c.3527_3549del (MSH6)	XP_024308587.1:p.Arg1176AsnfsTer4
XM_024452820.1:c.3344_3366del (MSH6)	XP_024308588.1:p.Arg1115AsnfsTer4
XM_024452821.1:c.3230_3252del (MSH6)	XP_024308589.1:p.Arg1077AsnfsTer4
XM_024452822.1:c.2621_2643del (MSH6)	XP_024308590.1:p.Arg874AsnfsTer4
NM_000179.3:c.3527_3549del (MSH6) MANE Select	NP_000170.1:p.Arg1176AsnfsTer4
NM_001281492.2:c.3137_3159del (MSH6)	NP_001268421.1:p.Arg1046AsnfsTer4
NM_001281493.2:c.2621_2643del (MSH6)	NP_001268422.1:p.Arg874AsnfsTer4
NM_001281494.2:c.2621_2643del (MSH6)	NP_001268423.1:p.Arg874AsnfsTer4