Canonical Allele Identifier: CA2658967946

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806380_47806397del , CM000664.2:g.47806380_47806397del GRCh38
NC_000002.11:g.48033519_48033536del , CM000664.1:g.48033519_48033536del GRCh37
NC_000002.10:g.47887023_47887040del NCBI36
NG_007111.1:g.28234_28251del , LRG_219:g.28234_28251del
NG_008397.1:g.104285_104302del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3504+22_3504+39del (MSH6) ENSP00000406248.2:n.3504+22_3504+39del
ENST00000420813.6:c.3504+22_3504+39del (MSH6) ENSP00000390382.2:n.3504+22_3504+39del
ENST00000455383.6:c.3504+22_3504+39del (MSH6) ENSP00000397484.2:n.3504+22_3504+39del
ENST00000700004.2:c.3417+22_3417+39del (MSH6) ENSP00000514752.2:n.3417+22_3417+39del
ENST00000699999.1:n.4475+22_4475+39del (MSH6)
ENST00000700000.1:c.2235+22_2235+39del (MSH6) ENSP00000514749.1:n.2235+22_2235+39del
ENST00000700002.1:c.3807+22_3807+39del (MSH6) ENSP00000514750.1:n.3807+22_3807+39del
ENST00000700003.1:c.1256+22_1256+39del (MSH6) ENSP00000514751.1:n.1256+22_1256+39del
ENST00000700004.1:c.2574+22_2574+39del (MSH6) ENSP00000514752.1:n.2574+22_2574+39del
ENST00000700005.1:n.2652+22_2652+39del (MSH6)
ENST00000700006.1:n.4959+22_4959+39del (MSH6)
ENST00000700007.1:n.2396+22_2396+39del (MSH6)
ENST00000700008.1:n.1992_2009del (MSH6)
ENST00000700009.1:n.2465+22_2465+39del (MSH6)
ENST00000700010.1:n.1210+22_1210+39del (MSH6)
ENST00000700011.1:n.3095+22_3095+39del (MSH6)
ENST00000682451.1:n.4357_4374del (FBXO11)
ENST00000684712.1:n.4619_4636del (FBXO11)
ENST00000234420.11:c.3801+22_3801+39del (MSH6) MANE Select ENSP00000234420.5:n.3801+22_3801+39del
ENST00000540021.6:c.3411+22_3411+39del (MSH6) ENSP00000446475.1:n.3411+22_3411+39del
ENST00000652107.1:c.3504+22_3504+39del (MSH6) ENSP00000498629.1:n.3504+22_3504+39del
ENST00000673637.1:c.3504+22_3504+39del (MSH6) ENSP00000501310.1:n.3504+22_3504+39del
ENST00000234420.9:c.3801+22_3801+39del (MSH6) ENSP00000234420.4:n.3801+22_3801+39del
ENST00000405808.5:c.169+1804_169+1821del (FBXO11) ENSP00000385127.1:n.169+1804_169+1821del
ENST00000434234.5:c.*124+1603_*124+1620del (FBXO11) ENSP00000402692.1:n.*124+1603_*124+1620del
ENST00000445503.5:c.*3148+22_*3148+39del (MSH6) ENSP00000405294.1:n.*3148+22_*3148+39del
ENST00000538136.1:c.2895+22_2895+39del (MSH6) ENSP00000438580.1:n.2895+22_2895+39del
ENST00000540021.5:c.3411+22_3411+39del (MSH6) ENSP00000446475.1:n.3411+22_3411+39del
ENST00000614496.4:c.2895+22_2895+39del (MSH6) ENSP00000477844.1:n.2895+22_2895+39del
ENST00000622629.4:c.702+22_702+39del (MSH6) ENSP00000482078.1:n.702+22_702+39del
NM_000179.2:c.3801+22_3801+39del , LRG_219t1:c.3801+22_3801+39del (MSH6) NP_000170.1:n.3801+22_3801+39del
NM_001281492.1:c.3411+22_3411+39del (MSH6) NP_001268421.1:n.3411+22_3411+39del
NM_001281493.1:c.2895+22_2895+39del (MSH6) NP_001268422.1:n.2895+22_2895+39del
NM_001281494.1:c.2895+22_2895+39del (MSH6) NP_001268423.1:n.2895+22_2895+39del
XM_005264271.1:c.3504+22_3504+39del (MSH6) XP_005264328.1:n.3504+22_3504+39del
XM_011532798.1:c.3618+22_3618+39del (MSH6) XP_011531100.1:n.3618+22_3618+39del
XM_011532799.1:c.3504+22_3504+39del (MSH6) XP_011531101.1:n.3504+22_3504+39del
XM_011532800.1:c.3504+22_3504+39del (MSH6) XP_011531102.1:n.3504+22_3504+39del
XM_024452819.1:c.3823_3840del (MSH6) XP_024308587.1:p.Pro1275_Phe1280del
XM_024452820.1:c.3640_3657del (MSH6) XP_024308588.1:p.Pro1214_Phe1219del
XM_024452821.1:c.3526_3543del (MSH6) XP_024308589.1:p.Pro1176_Phe1181del
XM_024452822.1:c.2917_2934del (MSH6) XP_024308590.1:p.Pro973_Phe978del
NM_000179.3:c.3801+22_3801+39del (MSH6) MANE Select NP_000170.1:n.3801+22_3801+39del
NM_001281492.2:c.3411+22_3411+39del (MSH6) NP_001268421.1:n.3411+22_3411+39del
NM_001281493.2:c.2895+22_2895+39del (MSH6) NP_001268422.1:n.2895+22_2895+39del
NM_001281494.2:c.2895+22_2895+39del (MSH6) NP_001268423.1:n.2895+22_2895+39del