Canonical Allele Identifier: CA2586964953

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804995_47804997del , CM000664.2:g.47804995_47804997del	GRCh38
NC_000002.11:g.48032134_48032136del , CM000664.1:g.48032134_48032136del	GRCh37
NC_000002.10:g.47885638_47885640del	NCBI36
NG_007111.1:g.26849_26851del , LRG_219:g.26849_26851del
NG_008397.1:g.105681_105683del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3227_3229del (MSH6)	ENSP00000406248.2:p.Thr1076del
ENST00000420813.6:c.3227_3229del (MSH6)	ENSP00000390382.2:p.Thr1076del
ENST00000455383.6:c.3227_3229del (MSH6)	ENSP00000397484.2:p.Thr1076del
ENST00000700004.2:c.3173-623_3173-621del (MSH6)	ENSP00000514752.2:n.3173-623_3173-621del
ENST00000699999.1:n.3608_3610del (MSH6)
ENST00000700000.1:c.1958_1960del (MSH6)	ENSP00000514749.1:p.Thr653del
ENST00000700002.1:c.3530_3532del (MSH6)	ENSP00000514750.1:p.Thr1177del
ENST00000700003.1:c.979_981del (MSH6)	ENSP00000514751.1:n.979_981del
ENST00000700004.1:c.2330-623_2330-621del (MSH6)	ENSP00000514752.1:n.2330-623_2330-621del
ENST00000700005.1:n.2375_2377del (MSH6)
ENST00000700006.1:n.3596_3598del (MSH6)
ENST00000700007.1:n.1529_1531del (MSH6)
ENST00000700008.1:n.1103_1105del (MSH6)
ENST00000700009.1:n.1102_1104del (MSH6)
ENST00000700010.1:n.933_935del (MSH6)
ENST00000700011.1:n.2228_2230del (MSH6)
ENST00000234420.11:c.3524_3526del (MSH6) MANE Select	ENSP00000234420.5:p.Thr1175del
ENST00000540021.6:c.3134_3136del (MSH6)	ENSP00000446475.1:p.Thr1045del
ENST00000652107.1:c.3227_3229del (MSH6)	ENSP00000498629.1:p.Thr1076del
ENST00000673637.1:c.3227_3229del (MSH6)	ENSP00000501310.1:p.Thr1076del
ENST00000234420.9:c.3524_3526del (MSH6)	ENSP00000234420.4:p.Thr1175del
ENST00000405808.5:c.169+3200_169+3202del (FBXO11)	ENSP00000385127.1:n.169+3200_169+3202del
ENST00000434234.5:c.*124+2999_*124+3001del (FBXO11)	ENSP00000402692.1:n.*124+2999_*124+3001de...
ENST00000445503.5:c.*2871_*2873del (MSH6)	ENSP00000405294.1:n.*2871_*2873del
ENST00000538136.1:c.2618_2620del (MSH6)	ENSP00000438580.1:p.Thr873del
ENST00000540021.5:c.3134_3136del (MSH6)	ENSP00000446475.1:p.Thr1045del
ENST00000614496.4:c.2618_2620del (MSH6)	ENSP00000477844.1:p.Thr873del
ENST00000622629.4:c.428_430del (MSH6)	ENSP00000482078.1:p.Thr143del
NM_000179.2:c.3524_3526del , LRG_219t1:c.3524_3526del (MSH6)	NP_000170.1:p.Thr1175del
NM_001281492.1:c.3134_3136del (MSH6)	NP_001268421.1:p.Thr1045del
NM_001281493.1:c.2618_2620del (MSH6)	NP_001268422.1:p.Thr873del
NM_001281494.1:c.2618_2620del (MSH6)	NP_001268423.1:p.Thr873del
XM_005264271.1:c.3227_3229del (MSH6)	XP_005264328.1:p.Thr1076del
XM_011532798.1:c.3341_3343del (MSH6)	XP_011531100.1:p.Thr1114del
XM_011532799.1:c.3227_3229del (MSH6)	XP_011531101.1:p.Thr1076del
XM_011532800.1:c.3227_3229del (MSH6)	XP_011531102.1:p.Thr1076del
XM_024452819.1:c.3524_3526del (MSH6)	XP_024308587.1:p.Thr1175del
XM_024452820.1:c.3341_3343del (MSH6)	XP_024308588.1:p.Thr1114del
XM_024452821.1:c.3227_3229del (MSH6)	XP_024308589.1:p.Thr1076del
XM_024452822.1:c.2618_2620del (MSH6)	XP_024308590.1:p.Thr873del
NM_000179.3:c.3524_3526del (MSH6) MANE Select	NP_000170.1:p.Thr1175del
NM_001281492.2:c.3134_3136del (MSH6)	NP_001268421.1:p.Thr1045del
NM_001281493.2:c.2618_2620del (MSH6)	NP_001268422.1:p.Thr873del
NM_001281494.2:c.2618_2620del (MSH6)	NP_001268423.1:p.Thr873del