Canonical Allele Identifier: CA2496053185

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805268_47805269delinsCT , CM000664.2:g.47805268_47805269delinsCT	GRCh38
NC_000002.11:g.48032407_48032408delinsCT , CM000664.1:g.48032407_48032408delinsCT	GRCh37
NC_000002.10:g.47885911_47885912delinsCT	NCBI36
NG_007111.1:g.27122_27123delinsCT , LRG_219:g.27122_27123delinsCT
NG_008397.1:g.105407_105408delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3259+241_3259+242delinsCT (MSH6)	ENSP00000406248.2:n.3259+241_3259+242delinsCT
ENST00000420813.6:c.3259+241_3259+242delinsCT (MSH6)	ENSP00000390382.2:n.3259+241_3259+242delinsCT
ENST00000455383.6:c.3259+241_3259+242delinsCT (MSH6)	ENSP00000397484.2:n.3259+241_3259+242delinsCT
ENST00000700004.2:c.3173-350_3173-349delinsCT (MSH6)	ENSP00000514752.2:n.3173-350_3173-349delinsCT
ENST00000699999.1:n.3881_3882delinsCT (MSH6)
ENST00000700000.1:c.1990+241_1990+242delinsCT (MSH6)	ENSP00000514749.1:n.1990+241_1990+242delinsCT
ENST00000700002.1:c.3562+241_3562+242delinsCT (MSH6)	ENSP00000514750.1:n.3562+241_3562+242delinsCT
ENST00000700003.1:c.1011+241_1011+242delinsCT (MSH6)	ENSP00000514751.1:n.1011+241_1011+242delinsCT
ENST00000700004.1:c.2330-350_2330-349delinsCT (MSH6)	ENSP00000514752.1:n.2330-350_2330-349delinsCT
ENST00000700005.1:n.2407+241_2407+242delinsCT (MSH6)
ENST00000700006.1:n.3869_3870delinsCT (MSH6)
ENST00000700007.1:n.1802_1803delinsCT (MSH6)
ENST00000700008.1:n.1376_1377delinsCT (MSH6)
ENST00000700009.1:n.1375_1376delinsCT (MSH6)
ENST00000700010.1:n.965+241_965+242delinsCT (MSH6)
ENST00000700011.1:n.2501_2502delinsCT (MSH6)
ENST00000234420.11:c.3556+241_3556+242delinsCT (MSH6) MANE Select	ENSP00000234420.5:n.3556+241_3556+242delinsCT
ENST00000540021.6:c.3166+241_3166+242delinsCT (MSH6)	ENSP00000446475.1:n.3166+241_3166+242delinsCT
ENST00000652107.1:c.3259+241_3259+242delinsCT (MSH6)	ENSP00000498629.1:n.3259+241_3259+242delinsCT
ENST00000673637.1:c.3259+241_3259+242delinsCT (MSH6)	ENSP00000501310.1:n.3259+241_3259+242delinsCT
ENST00000234420.9:c.3556+241_3556+242delinsCT (MSH6)	ENSP00000234420.4:n.3556+241_3556+242delinsCT
ENST00000405808.5:c.169+2926_169+2927delinsAG (FBXO11)	ENSP00000385127.1:n.169+2926_169+2927delinsAG
ENST00000434234.5:c.*124+2725_*124+2726delinsAG (FBXO11)	ENSP00000402692.1:n.*124+2725_*124+2726delinsAG
ENST00000445503.5:c.*2903+241_*2903+242delinsCT (MSH6)	ENSP00000405294.1:n.*2903+241_*2903+242delinsCT
ENST00000538136.1:c.2650+241_2650+242delinsCT (MSH6)	ENSP00000438580.1:n.2650+241_2650+242delinsCT
ENST00000540021.5:c.3166+241_3166+242delinsCT (MSH6)	ENSP00000446475.1:n.3166+241_3166+242delinsCT
ENST00000614496.4:c.2650+241_2650+242delinsCT (MSH6)	ENSP00000477844.1:n.2650+241_2650+242delinsCT
ENST00000622629.4:c.460+241_460+242delinsCT (MSH6)	ENSP00000482078.1:n.460+241_460+242delinsCT
NM_000179.2:c.3556+241_3556+242delinsCT , LRG_219t1:c.3556+241_3556+242delinsCT (MSH6)	NP_000170.1:n.3556+241_3556+242delinsCT
NM_001281492.1:c.3166+241_3166+242delinsCT (MSH6)	NP_001268421.1:n.3166+241_3166+242delinsCT
NM_001281493.1:c.2650+241_2650+242delinsCT (MSH6)	NP_001268422.1:n.2650+241_2650+242delinsCT
NM_001281494.1:c.2650+241_2650+242delinsCT (MSH6)	NP_001268423.1:n.2650+241_2650+242delinsCT
XM_005264271.1:c.3259+241_3259+242delinsCT (MSH6)	XP_005264328.1:n.3259+241_3259+242delinsCT
XM_011532798.1:c.3373+241_3373+242delinsCT (MSH6)	XP_011531100.1:n.3373+241_3373+242delinsCT
XM_011532799.1:c.3259+241_3259+242delinsCT (MSH6)	XP_011531101.1:n.3259+241_3259+242delinsCT
XM_011532800.1:c.3259+241_3259+242delinsCT (MSH6)	XP_011531102.1:n.3259+241_3259+242delinsCT
XM_024452819.1:c.3556+241_3556+242delinsCT (MSH6)	XP_024308587.1:n.3556+241_3556+242delinsCT
XM_024452820.1:c.3373+241_3373+242delinsCT (MSH6)	XP_024308588.1:n.3373+241_3373+242delinsCT
XM_024452821.1:c.3259+241_3259+242delinsCT (MSH6)	XP_024308589.1:n.3259+241_3259+242delinsCT
XM_024452822.1:c.2650+241_2650+242delinsCT (MSH6)	XP_024308590.1:n.2650+241_2650+242delinsCT
NM_000179.3:c.3556+241_3556+242delinsCT (MSH6) MANE Select	NP_000170.1:n.3556+241_3556+242delinsCT
NM_001281492.2:c.3166+241_3166+242delinsCT (MSH6)	NP_001268421.1:n.3166+241_3166+242delinsCT
NM_001281493.2:c.2650+241_2650+242delinsCT (MSH6)	NP_001268422.1:n.2650+241_2650+242delinsCT
NM_001281494.2:c.2650+241_2650+242delinsCT (MSH6)	NP_001268423.1:n.2650+241_2650+242delinsCT