Canonical Allele Identifier: CA913187995

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 919005
• ClinVar RCV Id: RCV001176929
• dbSNP Id: rs1669885163

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805048_47805049del , CM000664.2:g.47805048_47805049del	GRCh38
NC_000002.11:g.48032187_48032188del , CM000664.1:g.48032187_48032188del	GRCh37
NC_000002.10:g.47885691_47885692del	NCBI36
NG_007111.1:g.26902_26903del , LRG_219:g.26902_26903del
NG_008397.1:g.105627_105628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3259+21_3259+22del (MSH6)	ENSP00000406248.2:n.3259+21_3259+22del
ENST00000420813.6:c.3259+21_3259+22del (MSH6)	ENSP00000390382.2:n.3259+21_3259+22del
ENST00000455383.6:c.3259+21_3259+22del (MSH6)	ENSP00000397484.2:n.3259+21_3259+22del
ENST00000700004.2:c.3173-570_3173-569del (MSH6)	ENSP00000514752.2:n.3173-570_3173-569del
ENST00000699999.1:n.3661_3662del (MSH6)
ENST00000700000.1:c.1990+21_1990+22del (MSH6)	ENSP00000514749.1:n.1990+21_1990+22del
ENST00000700002.1:c.3562+21_3562+22del (MSH6)	ENSP00000514750.1:n.3562+21_3562+22del
ENST00000700003.1:c.1011+21_1011+22del (MSH6)	ENSP00000514751.1:n.1011+21_1011+22del
ENST00000700004.1:c.2330-570_2330-569del (MSH6)	ENSP00000514752.1:n.2330-570_2330-569del
ENST00000700005.1:n.2407+21_2407+22del (MSH6)
ENST00000700006.1:n.3649_3650del (MSH6)
ENST00000700007.1:n.1582_1583del (MSH6)
ENST00000700008.1:n.1156_1157del (MSH6)
ENST00000700009.1:n.1155_1156del (MSH6)
ENST00000700010.1:n.965+21_965+22del (MSH6)
ENST00000700011.1:n.2281_2282del (MSH6)
ENST00000234420.11:c.3556+21_3556+22del (MSH6) MANE Select	ENSP00000234420.5:n.3556+21_3556+22del
ENST00000540021.6:c.3166+21_3166+22del (MSH6)	ENSP00000446475.1:n.3166+21_3166+22del
ENST00000652107.1:c.3259+21_3259+22del (MSH6)	ENSP00000498629.1:n.3259+21_3259+22del
ENST00000673637.1:c.3259+21_3259+22del (MSH6)	ENSP00000501310.1:n.3259+21_3259+22del
ENST00000234420.9:c.3556+21_3556+22del (MSH6)	ENSP00000234420.4:n.3556+21_3556+22del
ENST00000405808.5:c.169+3146_169+3147del (FBXO11)	ENSP00000385127.1:n.169+3146_169+3147del
ENST00000434234.5:c.*124+2945_*124+2946del (FBXO11)	ENSP00000402692.1:n.*124+2945_*124+2946del
ENST00000445503.5:c.*2903+21_*2903+22del (MSH6)	ENSP00000405294.1:n.*2903+21_*2903+22del
ENST00000538136.1:c.2650+21_2650+22del (MSH6)	ENSP00000438580.1:n.2650+21_2650+22del
ENST00000540021.5:c.3166+21_3166+22del (MSH6)	ENSP00000446475.1:n.3166+21_3166+22del
ENST00000614496.4:c.2650+21_2650+22del (MSH6)	ENSP00000477844.1:n.2650+21_2650+22del
ENST00000622629.4:c.460+21_460+22del (MSH6)	ENSP00000482078.1:n.460+21_460+22del
NM_000179.2:c.3556+21_3556+22del , LRG_219t1:c.3556+21_3556+22del (MSH6)	NP_000170.1:n.3556+21_3556+22del
NM_001281492.1:c.3166+21_3166+22del (MSH6)	NP_001268421.1:n.3166+21_3166+22del
NM_001281493.1:c.2650+21_2650+22del (MSH6)	NP_001268422.1:n.2650+21_2650+22del
NM_001281494.1:c.2650+21_2650+22del (MSH6)	NP_001268423.1:n.2650+21_2650+22del
XM_005264271.1:c.3259+21_3259+22del (MSH6)	XP_005264328.1:n.3259+21_3259+22del
XM_011532798.1:c.3373+21_3373+22del (MSH6)	XP_011531100.1:n.3373+21_3373+22del
XM_011532799.1:c.3259+21_3259+22del (MSH6)	XP_011531101.1:n.3259+21_3259+22del
XM_011532800.1:c.3259+21_3259+22del (MSH6)	XP_011531102.1:n.3259+21_3259+22del
XM_024452819.1:c.3556+21_3556+22del (MSH6)	XP_024308587.1:n.3556+21_3556+22del
XM_024452820.1:c.3373+21_3373+22del (MSH6)	XP_024308588.1:n.3373+21_3373+22del
XM_024452821.1:c.3259+21_3259+22del (MSH6)	XP_024308589.1:n.3259+21_3259+22del
XM_024452822.1:c.2650+21_2650+22del (MSH6)	XP_024308590.1:n.2650+21_2650+22del
NM_000179.3:c.3556+21_3556+22del (MSH6) MANE Select	NP_000170.1:n.3556+21_3556+22del
NM_001281492.2:c.3166+21_3166+22del (MSH6)	NP_001268421.1:n.3166+21_3166+22del
NM_001281493.2:c.2650+21_2650+22del (MSH6)	NP_001268422.1:n.2650+21_2650+22del
NM_001281494.2:c.2650+21_2650+22del (MSH6)	NP_001268423.1:n.2650+21_2650+22del