Canonical Allele Identifier: CA1649475

Linked Data

dbSNP Id: rs750924940

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806340_47806362dup , CM000664.2:g.47806340_47806362dup GRCh38
NC_000002.11:g.48033479_48033501dup , CM000664.1:g.48033479_48033501dup GRCh37
NC_000002.10:g.47886983_47887005dup NCBI36
NG_007111.1:g.28194_28216dup , LRG_219:g.28194_28216dup
NG_008397.1:g.104314_104336dup

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3486_3504+4dup (MSH6)
ENST00000420813.6:c.3486_3504+4dup (MSH6)
ENST00000455383.6:c.3486_3504+4dup (MSH6)
ENST00000700004.2:c.3399_3417+4dup (MSH6)
ENST00000699999.1:n.4457_4475+4dup (MSH6)
ENST00000700000.1:c.2217_2235+4dup (MSH6)
ENST00000700002.1:c.3789_3807+4dup (MSH6)
ENST00000700003.1:c.1238_1256+4dup (MSH6)
ENST00000700004.1:c.2556_2574+4dup (MSH6)
ENST00000700005.1:n.2634_2652+4dup (MSH6)
ENST00000700006.1:n.4941_4959+4dup (MSH6)
ENST00000700007.1:n.2378_2396+4dup (MSH6)
ENST00000700008.1:n.1952_1974dup (MSH6)
ENST00000700009.1:n.2447_2465+4dup (MSH6)
ENST00000700010.1:n.1192_1210+4dup (MSH6)
ENST00000700011.1:n.3077_3095+4dup (MSH6)
ENST00000682451.1:n.4386_4408dup (FBXO11)
ENST00000684712.1:n.4648_4670dup (FBXO11)
ENST00000234420.11:c.3783_3801+4dup (MSH6)
ENST00000540021.6:c.3393_3411+4dup (MSH6)
ENST00000652107.1:c.3486_3504+4dup (MSH6)
ENST00000673637.1:c.3486_3504+4dup (MSH6)
ENST00000234420.9:c.3783_3801+4dup (MSH6)
ENST00000405808.5:c.169+1833_169+1855dup (FBXO11) ENSP00000385127.1:n.169+1833_169+1855dup
ENST00000434234.5:c.*124+1632_*124+1654dup (FBXO11) ENSP00000402692.1:n.*124+1632_*124+1654du...
ENST00000445503.5:c.*3130_*3148+4dup (MSH6)
ENST00000538136.1:c.2877_2895+4dup (MSH6)
ENST00000540021.5:c.3393_3411+4dup (MSH6)
ENST00000614496.4:c.2877_2895+4dup (MSH6)
ENST00000622629.4:c.685_702+4dup (MSH6)
NM_000179.2:c.3783_3801+4dup , LRG_219t1:c.3783_3801+4dup (MSH6)
NM_001281492.1:c.3393_3411+4dup (MSH6)
NM_001281493.1:c.2877_2895+4dup (MSH6)
NM_001281494.1:c.2877_2895+4dup (MSH6)
XM_005264271.1:c.3486_3504+4dup (MSH6)
XM_011532798.1:c.3600_3618+4dup (MSH6)
XM_011532799.1:c.3486_3504+4dup (MSH6)
XM_011532800.1:c.3486_3504+4dup (MSH6)
XM_024452819.1:c.3783_3805dup (MSH6) XP_024308587.1:p.Cys1269LeufsTer4
XM_024452820.1:c.3600_3622dup (MSH6) XP_024308588.1:p.Cys1208LeufsTer4
XM_024452821.1:c.3486_3508dup (MSH6) XP_024308589.1:p.Cys1170LeufsTer4
XM_024452822.1:c.2877_2899dup (MSH6) XP_024308590.1:p.Cys967LeufsTer4
NM_000179.3:c.3783_3801+4dup (MSH6)
NM_001281492.2:c.3393_3411+4dup (MSH6)
NM_001281493.2:c.2877_2895+4dup (MSH6)
NM_001281494.2:c.2877_2895+4dup (MSH6)