Canonical Allele Identifier: CA2586964890

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806323_47806338del , CM000664.2:g.47806323_47806338del	GRCh38
NC_000002.11:g.48033462_48033477del , CM000664.1:g.48033462_48033477del	GRCh37
NC_000002.10:g.47886966_47886981del	NCBI36
NG_007111.1:g.28177_28192del , LRG_219:g.28177_28192del
NG_008397.1:g.104338_104353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3469_3484del (MSH6)	ENSP00000406248.2:p.Tyr1157LeufsTer4
ENST00000420813.6:c.3469_3484del (MSH6)	ENSP00000390382.2:p.Tyr1157LeufsTer4
ENST00000455383.6:c.3469_3484del (MSH6)	ENSP00000397484.2:p.Tyr1157LeufsTer4
ENST00000700004.2:c.3382_3397del (MSH6)	ENSP00000514752.2:p.Tyr1128LeufsTer4
ENST00000699999.1:n.4440_4455del (MSH6)
ENST00000700000.1:c.2200_2215del (MSH6)	ENSP00000514749.1:p.Tyr734LeufsTer4
ENST00000700002.1:c.3772_3787del (MSH6)	ENSP00000514750.1:p.Tyr1258LeufsTer4
ENST00000700003.1:c.1221_1236del (MSH6)	ENSP00000514751.1:n.1221_1236del
ENST00000700004.1:c.2539_2554del (MSH6)	ENSP00000514752.1:p.Tyr847LeufsTer4
ENST00000700005.1:n.2617_2632del (MSH6)
ENST00000700006.1:n.4924_4939del (MSH6)
ENST00000700007.1:n.2361_2376del (MSH6)
ENST00000700008.1:n.1935_1950del (MSH6)
ENST00000700009.1:n.2430_2445del (MSH6)
ENST00000700010.1:n.1175_1190del (MSH6)
ENST00000700011.1:n.3060_3075del (MSH6)
ENST00000682451.1:n.4410_4425del (FBXO11)
ENST00000684712.1:n.4672_4687del (FBXO11)
ENST00000234420.11:c.3766_3781del (MSH6) MANE Select	ENSP00000234420.5:p.Tyr1256LeufsTer4
ENST00000540021.6:c.3376_3391del (MSH6)	ENSP00000446475.1:p.Tyr1126LeufsTer4
ENST00000652107.1:c.3469_3484del (MSH6)	ENSP00000498629.1:p.Tyr1157LeufsTer4
ENST00000673637.1:c.3469_3484del (MSH6)	ENSP00000501310.1:p.Tyr1157LeufsTer4
ENST00000234420.9:c.3766_3781del (MSH6)	ENSP00000234420.4:p.Tyr1256LeufsTer4
ENST00000405808.5:c.169+1857_169+1872del (FBXO11)	ENSP00000385127.1:n.169+1857_169+1872del
ENST00000434234.5:c.*124+1656_*124+1671del (FBXO11)	ENSP00000402692.1:n.*124+1656_*124+1671del
ENST00000445503.5:c.*3113_*3128del (MSH6)	ENSP00000405294.1:n.*3113_*3128del
ENST00000538136.1:c.2860_2875del (MSH6)	ENSP00000438580.1:p.Tyr954LeufsTer4
ENST00000540021.5:c.3376_3391del (MSH6)	ENSP00000446475.1:p.Tyr1126LeufsTer4
ENST00000614496.4:c.2860_2875del (MSH6)	ENSP00000477844.1:p.Tyr954LeufsTer4
ENST00000622629.4:c.668_683del (MSH6)	ENSP00000482078.1:p.Leu223SerfsTer4
NM_000179.2:c.3766_3781del , LRG_219t1:c.3766_3781del (MSH6)	NP_000170.1:p.Tyr1256LeufsTer4
NM_001281492.1:c.3376_3391del (MSH6)	NP_001268421.1:p.Tyr1126LeufsTer4
NM_001281493.1:c.2860_2875del (MSH6)	NP_001268422.1:p.Tyr954LeufsTer4
NM_001281494.1:c.2860_2875del (MSH6)	NP_001268423.1:p.Tyr954LeufsTer4
XM_005264271.1:c.3469_3484del (MSH6)	XP_005264328.1:p.Tyr1157LeufsTer4
XM_011532798.1:c.3583_3598del (MSH6)	XP_011531100.1:p.Tyr1195LeufsTer4
XM_011532799.1:c.3469_3484del (MSH6)	XP_011531101.1:p.Tyr1157LeufsTer4
XM_011532800.1:c.3469_3484del (MSH6)	XP_011531102.1:p.Tyr1157LeufsTer4
XM_024452819.1:c.3766_3781del (MSH6)	XP_024308587.1:p.Tyr1256LeufsTer4
XM_024452820.1:c.3583_3598del (MSH6)	XP_024308588.1:p.Tyr1195LeufsTer4
XM_024452821.1:c.3469_3484del (MSH6)	XP_024308589.1:p.Tyr1157LeufsTer4
XM_024452822.1:c.2860_2875del (MSH6)	XP_024308590.1:p.Tyr954LeufsTer4
NM_000179.3:c.3766_3781del (MSH6) MANE Select	NP_000170.1:p.Tyr1256LeufsTer4
NM_001281492.2:c.3376_3391del (MSH6)	NP_001268421.1:p.Tyr1126LeufsTer4
NM_001281493.2:c.2860_2875del (MSH6)	NP_001268422.1:p.Tyr954LeufsTer4
NM_001281494.2:c.2860_2875del (MSH6)	NP_001268423.1:p.Tyr954LeufsTer4