Canonical Allele Identifier: CA2580067277

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1733817
• ClinVar RCV Id: RCV002452676

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806231_47806247del , CM000664.2:g.47806231_47806247del	GRCh38
NC_000002.11:g.48033370_48033386del , CM000664.1:g.48033370_48033386del	GRCh37
NC_000002.10:g.47886874_47886890del	NCBI36
NG_007111.1:g.28085_28101del , LRG_219:g.28085_28101del
NG_008397.1:g.104430_104446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3377_3393del (MSH6)	ENSP00000406248.2:p.Thr1126SerfsTer3
ENST00000420813.6:c.3377_3393del (MSH6)	ENSP00000390382.2:p.Thr1126SerfsTer3
ENST00000455383.6:c.3377_3393del (MSH6)	ENSP00000397484.2:p.Thr1126SerfsTer3
ENST00000700004.2:c.3290_3306del (MSH6)	ENSP00000514752.2:p.Thr1097SerfsTer3
ENST00000699999.1:n.4348_4364del (MSH6)
ENST00000700000.1:c.2108_2124del (MSH6)	ENSP00000514749.1:p.Thr703SerfsTer3
ENST00000700002.1:c.3680_3696del (MSH6)	ENSP00000514750.1:p.Thr1227SerfsTer3
ENST00000700003.1:c.1129_1145del (MSH6)	ENSP00000514751.1:n.1129_1145del
ENST00000700004.1:c.2447_2463del (MSH6)	ENSP00000514752.1:p.Thr816SerfsTer3
ENST00000700005.1:n.2525_2541del (MSH6)
ENST00000700006.1:n.4832_4848del (MSH6)
ENST00000700007.1:n.2269_2285del (MSH6)
ENST00000700008.1:n.1843_1859del (MSH6)
ENST00000700009.1:n.2338_2354del (MSH6)
ENST00000700010.1:n.1083_1099del (MSH6)
ENST00000700011.1:n.2968_2984del (MSH6)
ENST00000682451.1:n.4502_4518del (FBXO11)
ENST00000684712.1:n.4764_4780del (FBXO11)
ENST00000234420.11:c.3674_3690del (MSH6) MANE Select	ENSP00000234420.5:p.Thr1225SerfsTer3
ENST00000540021.6:c.3284_3300del (MSH6)	ENSP00000446475.1:p.Thr1095SerfsTer3
ENST00000652107.1:c.3377_3393del (MSH6)	ENSP00000498629.1:p.Thr1126SerfsTer3
ENST00000673637.1:c.3377_3393del (MSH6)	ENSP00000501310.1:p.Thr1126SerfsTer3
ENST00000234420.9:c.3674_3690del (MSH6)	ENSP00000234420.4:p.Thr1225SerfsTer3
ENST00000405808.5:c.169+1949_169+1965del (FBXO11)	ENSP00000385127.1:n.169+1949_169+1965del
ENST00000434234.5:c.*124+1748_*124+1764del (FBXO11)	ENSP00000402692.1:n.*124+1748_*124+1764del
ENST00000445503.5:c.*3021_*3037del (MSH6)	ENSP00000405294.1:n.*3021_*3037del
ENST00000538136.1:c.2768_2784del (MSH6)	ENSP00000438580.1:p.Thr923SerfsTer3
ENST00000540021.5:c.3284_3300del (MSH6)	ENSP00000446475.1:p.Thr1095SerfsTer3
ENST00000614496.4:c.2768_2784del (MSH6)	ENSP00000477844.1:p.Thr923SerfsTer3
ENST00000622629.4:c.578_594del (MSH6)	ENSP00000482078.1:p.Thr193SerfsTer3
NM_000179.2:c.3674_3690del , LRG_219t1:c.3674_3690del (MSH6)	NP_000170.1:p.Thr1225SerfsTer3
NM_001281492.1:c.3284_3300del (MSH6)	NP_001268421.1:p.Thr1095SerfsTer3
NM_001281493.1:c.2768_2784del (MSH6)	NP_001268422.1:p.Thr923SerfsTer3
NM_001281494.1:c.2768_2784del (MSH6)	NP_001268423.1:p.Thr923SerfsTer3
XM_005264271.1:c.3377_3393del (MSH6)	XP_005264328.1:p.Thr1126SerfsTer3
XM_011532798.1:c.3491_3507del (MSH6)	XP_011531100.1:p.Thr1164SerfsTer3
XM_011532799.1:c.3377_3393del (MSH6)	XP_011531101.1:p.Thr1126SerfsTer3
XM_011532800.1:c.3377_3393del (MSH6)	XP_011531102.1:p.Thr1126SerfsTer3
XM_024452819.1:c.3674_3690del (MSH6)	XP_024308587.1:p.Thr1225SerfsTer3
XM_024452820.1:c.3491_3507del (MSH6)	XP_024308588.1:p.Thr1164SerfsTer3
XM_024452821.1:c.3377_3393del (MSH6)	XP_024308589.1:p.Thr1126SerfsTer3
XM_024452822.1:c.2768_2784del (MSH6)	XP_024308590.1:p.Thr923SerfsTer3
NM_000179.3:c.3674_3690del (MSH6) MANE Select	NP_000170.1:p.Thr1225SerfsTer3
NM_001281492.2:c.3284_3300del (MSH6)	NP_001268421.1:p.Thr1095SerfsTer3
NM_001281493.2:c.2768_2784del (MSH6)	NP_001268422.1:p.Thr923SerfsTer3
NM_001281494.2:c.2768_2784del (MSH6)	NP_001268423.1:p.Thr923SerfsTer3