Canonical Allele Identifier: CA2658966748

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47805620_47805624del , CM000664.2:g.47805620_47805624del GRCh38
NC_000002.11:g.48032759_48032763del , CM000664.1:g.48032759_48032763del GRCh37
NC_000002.10:g.47886263_47886267del NCBI36
NG_007111.1:g.27474_27478del , LRG_219:g.27474_27478del
NG_008397.1:g.105052_105056del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3262_3266del (MSH6) ENSP00000406248.2:p.Glu1088TyrfsTer5
ENST00000420813.6:c.3262_3266del (MSH6) ENSP00000390382.2:p.Glu1088TyrfsTer5
ENST00000455383.6:c.3262_3266del (MSH6) ENSP00000397484.2:p.Glu1088TyrfsTer5
ENST00000700004.2:c.3175_3179del (MSH6) ENSP00000514752.2:p.Glu1059TyrfsTer5
ENST00000699999.1:n.4233_4237del (MSH6)
ENST00000700000.1:c.1993_1997del (MSH6) ENSP00000514749.1:p.Glu665TyrfsTer5
ENST00000700002.1:c.3565_3569del (MSH6) ENSP00000514750.1:p.Glu1189TyrfsTer5
ENST00000700003.1:c.1014_1018del (MSH6) ENSP00000514751.1:n.1014_1018del
ENST00000700004.1:c.2332_2336del (MSH6) ENSP00000514752.1:p.Glu778TyrfsTer5
ENST00000700005.1:n.2410_2414del (MSH6)
ENST00000700006.1:n.4221_4225del (MSH6)
ENST00000700007.1:n.2154_2158del (MSH6)
ENST00000700008.1:n.1728_1732del (MSH6)
ENST00000700009.1:n.1727_1731del (MSH6)
ENST00000700010.1:n.968_972del (MSH6)
ENST00000700011.1:n.2853_2857del (MSH6)
ENST00000234420.11:c.3559_3563del (MSH6) MANE Select ENSP00000234420.5:p.Glu1187TyrfsTer5
ENST00000540021.6:c.3169_3173del (MSH6) ENSP00000446475.1:p.Glu1057TyrfsTer5
ENST00000652107.1:c.3262_3266del (MSH6) ENSP00000498629.1:p.Glu1088TyrfsTer5
ENST00000673637.1:c.3262_3266del (MSH6) ENSP00000501310.1:p.Glu1088TyrfsTer5
ENST00000234420.9:c.3559_3563del (MSH6) ENSP00000234420.4:p.Glu1187TyrfsTer5
ENST00000405808.5:c.169+2571_169+2575del (FBXO11) ENSP00000385127.1:n.169+2571_169+2575del
ENST00000434234.5:c.*124+2370_*124+2374del (FBXO11) ENSP00000402692.1:n.*124+2370_*124+2374del
ENST00000445503.5:c.*2906_*2910del (MSH6) ENSP00000405294.1:n.*2906_*2910del
ENST00000538136.1:c.2653_2657del (MSH6) ENSP00000438580.1:p.Glu885TyrfsTer5
ENST00000540021.5:c.3169_3173del (MSH6) ENSP00000446475.1:p.Glu1057TyrfsTer5
ENST00000614496.4:c.2653_2657del (MSH6) ENSP00000477844.1:p.Glu885TyrfsTer5
ENST00000622629.4:c.463_467del (MSH6) ENSP00000482078.1:p.Glu155TyrfsTer5
NM_000179.2:c.3559_3563del , LRG_219t1:c.3559_3563del (MSH6) NP_000170.1:p.Glu1187TyrfsTer5
NM_001281492.1:c.3169_3173del (MSH6) NP_001268421.1:p.Glu1057TyrfsTer5
NM_001281493.1:c.2653_2657del (MSH6) NP_001268422.1:p.Glu885TyrfsTer5
NM_001281494.1:c.2653_2657del (MSH6) NP_001268423.1:p.Glu885TyrfsTer5
XM_005264271.1:c.3262_3266del (MSH6) XP_005264328.1:p.Glu1088TyrfsTer5
XM_011532798.1:c.3376_3380del (MSH6) XP_011531100.1:p.Glu1126TyrfsTer5
XM_011532799.1:c.3262_3266del (MSH6) XP_011531101.1:p.Glu1088TyrfsTer5
XM_011532800.1:c.3262_3266del (MSH6) XP_011531102.1:p.Glu1088TyrfsTer5
XM_024452819.1:c.3559_3563del (MSH6) XP_024308587.1:p.Glu1187TyrfsTer5
XM_024452820.1:c.3376_3380del (MSH6) XP_024308588.1:p.Glu1126TyrfsTer5
XM_024452821.1:c.3262_3266del (MSH6) XP_024308589.1:p.Glu1088TyrfsTer5
XM_024452822.1:c.2653_2657del (MSH6) XP_024308590.1:p.Glu885TyrfsTer5
NM_000179.3:c.3559_3563del (MSH6) MANE Select NP_000170.1:p.Glu1187TyrfsTer5
NM_001281492.2:c.3169_3173del (MSH6) NP_001268421.1:p.Glu1057TyrfsTer5
NM_001281493.2:c.2653_2657del (MSH6) NP_001268422.1:p.Glu885TyrfsTer5
NM_001281494.2:c.2653_2657del (MSH6) NP_001268423.1:p.Glu885TyrfsTer5