Canonical Allele Identifier: CA46715567
Gene: MSH6 HGNC NCBI
FBXO11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47803226_47803229del , CM000664.2:g.47803226_47803229del GRCh38
NC_000002.11:g.48030365_48030368del , CM000664.1:g.48030365_48030368del GRCh37
NC_000002.10:g.47883869_47883872del NCBI36
NG_007111.1:g.25080_25083del , LRG_219:g.25080_25083del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.2876-194_2876-191del (MSH6) ENSP00000406248.2:n.2876-194_2876-191del
ENST00000420813.6:c.2876-194_2876-191del (MSH6) ENSP00000390382.2:n.2876-194_2876-191del
ENST00000455383.6:c.2876-194_2876-191del (MSH6) ENSP00000397484.2:n.2876-194_2876-191del
ENST00000700004.2:c.3172+2071_3172+2074del (MSH6) ENSP00000514752.2:n.3172+2071_3172+2074del
ENST00000699999.1:n.3257-194_3257-191del (MSH6)
ENST00000700000.1:c.1607-194_1607-191del (MSH6) ENSP00000514749.1:n.1607-194_1607-191del
ENST00000700002.1:c.3179-194_3179-191del (MSH6) ENSP00000514750.1:n.3179-194_3179-191del
ENST00000700003.1:c.628-194_628-191del (MSH6) ENSP00000514751.1:n.628-194_628-191del
ENST00000700004.1:c.2329+2071_2329+2074del (MSH6) ENSP00000514752.1:n.2329+2071_2329+2074del
ENST00000700005.1:n.1830_1833del (MSH6)
ENST00000700006.1:n.1827_1830del (MSH6)
ENST00000700007.1:n.984_987del (MSH6)
ENST00000700008.1:n.558_561del (MSH6)
ENST00000700009.1:n.557_560del (MSH6)
ENST00000700010.1:n.536_539del (MSH6)
ENST00000700011.1:n.459_462del (MSH6)
ENST00000234420.11:c.3173-194_3173-191del (MSH6) MANE Select ENSP00000234420.5:n.3173-194_3173-191del
ENST00000540021.6:c.2783-194_2783-191del (MSH6) ENSP00000446475.1:n.2783-194_2783-191del
ENST00000652107.1:c.2876-194_2876-191del (MSH6) ENSP00000498629.1:n.2876-194_2876-191del
ENST00000673637.1:c.2876-194_2876-191del (MSH6) ENSP00000501310.1:n.2876-194_2876-191del
ENST00000234420.9:c.3173-194_3173-191del (MSH6) ENSP00000234420.4:n.3173-194_3173-191del
ENST00000405808.5:c.169+4969_169+4972del (FBXO11) ENSP00000385127.1:n.169+4969_169+4972del
ENST00000434234.5:c.*124+4768_*124+4771del (FBXO11) ENSP00000402692.1:n.*124+4768_*124+4771del
ENST00000445503.5:c.*2520-194_*2520-191del (MSH6) ENSP00000405294.1:n.*2520-194_*2520-191del
ENST00000538136.1:c.2267-194_2267-191del (MSH6) ENSP00000438580.1:n.2267-194_2267-191del
ENST00000540021.5:c.2783-194_2783-191del (MSH6) ENSP00000446475.1:n.2783-194_2783-191del
ENST00000614496.4:c.2267-194_2267-191del (MSH6) ENSP00000477844.1:n.2267-194_2267-191del
ENST00000622629.4:c.77-194_77-191del (MSH6) ENSP00000482078.1:n.77-194_77-191del
NM_000179.2:c.3173-194_3173-191del , LRG_219t1:c.3173-194_3173-191del (MSH6) NP_000170.1:n.3173-194_3173-191del
NM_001281492.1:c.2783-194_2783-191del (MSH6) NP_001268421.1:n.2783-194_2783-191del
NM_001281493.1:c.2267-194_2267-191del (MSH6) NP_001268422.1:n.2267-194_2267-191del
NM_001281494.1:c.2267-194_2267-191del (MSH6) NP_001268423.1:n.2267-194_2267-191del
XM_005264271.1:c.2876-194_2876-191del (MSH6) XP_005264328.1:n.2876-194_2876-191del
XM_011532798.1:c.2990-194_2990-191del (MSH6) XP_011531100.1:n.2990-194_2990-191del
XM_011532799.1:c.2876-194_2876-191del (MSH6) XP_011531101.1:n.2876-194_2876-191del
XM_011532800.1:c.2876-194_2876-191del (MSH6) XP_011531102.1:n.2876-194_2876-191del
XM_024452819.1:c.3173-194_3173-191del (MSH6) XP_024308587.1:n.3173-194_3173-191del
XM_024452820.1:c.2990-194_2990-191del (MSH6) XP_024308588.1:n.2990-194_2990-191del
XM_024452821.1:c.2876-194_2876-191del (MSH6) XP_024308589.1:n.2876-194_2876-191del
XM_024452822.1:c.2267-194_2267-191del (MSH6) XP_024308590.1:n.2267-194_2267-191del
NM_000179.3:c.3173-194_3173-191del (MSH6) MANE Select NP_000170.1:n.3173-194_3173-191del
NM_001281492.2:c.2783-194_2783-191del (MSH6) NP_001268421.1:n.2783-194_2783-191del
NM_001281493.2:c.2267-194_2267-191del (MSH6) NP_001268422.1:n.2267-194_2267-191del
NM_001281494.2:c.2267-194_2267-191del (MSH6) NP_001268423.1:n.2267-194_2267-191del
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