Canonical Allele Identifier: CA769468283

Linked Data

dbSNP Id: rs1354911081

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806710_47806715del , CM000664.2:g.47806710_47806715del GRCh38
NC_000002.11:g.48033849_48033854del , CM000664.1:g.48033849_48033854del GRCh37
NC_000002.10:g.47887353_47887358del NCBI36
NG_007111.1:g.28564_28569del , LRG_219:g.28564_28569del
NG_008397.1:g.103963_103968del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3704+59_3705-64del (MSH6) ENSP00000406248.2:n.3704+59_3705-64del
ENST00000420813.6:c.3704+59_3705-64del (MSH6) ENSP00000390382.2:n.3704+59_3705-64del
ENST00000455383.6:c.3704+59_3705-64del (MSH6) ENSP00000397484.2:n.3704+59_3705-64del
ENST00000700004.2:c.3617+59_3618-64del (MSH6) ENSP00000514752.2:n.3617+59_3618-64del
ENST00000699999.1:n.4675+59_4676-64del (MSH6)
ENST00000700000.1:c.2435+59_2436-64del (MSH6) ENSP00000514749.1:n.2435+59_2436-64del
ENST00000700002.1:c.4007+59_4008-64del (MSH6) ENSP00000514750.1:n.4007+59_4008-64del
ENST00000700003.1:c.1456+59_1457-64del (MSH6) ENSP00000514751.1:n.1456+59_1457-64del
ENST00000700004.1:c.2774+59_2775-64del (MSH6) ENSP00000514752.1:n.2774+59_2775-64del
ENST00000700005.1:n.2911_2916del (MSH6)
ENST00000700006.1:n.5218_5223del (MSH6)
ENST00000700007.1:n.2596+59_2597-64del (MSH6)
ENST00000700008.1:n.2263+59_2264-64del (MSH6)
ENST00000700009.1:n.2665+59_2666-64del (MSH6)
ENST00000700010.1:n.1410+59_1411-64del (MSH6)
ENST00000700011.1:n.3295+59_3296-64del (MSH6)
ENST00000682451.1:n.4035_4040del (FBXO11)
ENST00000684712.1:n.4297_4302del (FBXO11)
ENST00000234420.11:c.4001+59_4002-64del (MSH6) MANE Select ENSP00000234420.5:n.4001+59_4002-64del
ENST00000540021.6:c.3611+59_3612-64del (MSH6) ENSP00000446475.1:n.3611+59_3612-64del
ENST00000652107.1:c.3704+59_3705-64del (MSH6) ENSP00000498629.1:n.3704+59_3705-64del
ENST00000673637.1:c.3704+59_3705-64del (MSH6) ENSP00000501310.1:n.3704+59_3705-64del
ENST00000234420.9:c.4001+59_4002-64del (MSH6) ENSP00000234420.4:n.4001+59_4002-64del
ENST00000405808.5:c.169+1482_169+1487del (FBXO11) ENSP00000385127.1:n.169+1482_169+1487del
ENST00000434234.5:c.*124+1281_*124+1286del (FBXO11) ENSP00000402692.1:n.*124+1281_*124+1286del
ENST00000445503.5:c.*3348+59_*3349-64del (MSH6) ENSP00000405294.1:n.*3348+59_*3349-64del
ENST00000538136.1:c.3095+59_3096-64del (MSH6) ENSP00000438580.1:n.3095+59_3096-64del
ENST00000540021.5:c.3611+59_3612-64del (MSH6) ENSP00000446475.1:n.3611+59_3612-64del
ENST00000614496.4:c.3095+59_3096-64del (MSH6) ENSP00000477844.1:n.3095+59_3096-64del
ENST00000622629.4:c.902+59_903-64del (MSH6) ENSP00000482078.1:n.902+59_903-64del
NM_000179.2:c.4001+59_4002-64del , LRG_219t1:c.4001+59_4002-64del (MSH6) NP_000170.1:n.4001+59_4002-64del
NM_001281492.1:c.3611+59_3612-64del (MSH6) NP_001268421.1:n.3611+59_3612-64del
NM_001281493.1:c.3095+59_3096-64del (MSH6) NP_001268422.1:n.3095+59_3096-64del
NM_001281494.1:c.3095+59_3096-64del (MSH6) NP_001268423.1:n.3095+59_3096-64del
XM_005264271.1:c.3704+59_3705-64del (MSH6) XP_005264328.1:n.3704+59_3705-64del
XM_011532798.1:c.3818+59_3819-64del (MSH6) XP_011531100.1:n.3818+59_3819-64del
XM_011532799.1:c.3704+59_3705-64del (MSH6) XP_011531101.1:n.3704+59_3705-64del
XM_011532800.1:c.3704+59_3705-64del (MSH6) XP_011531102.1:n.3704+59_3705-64del
XM_024452819.1:c.4094+59_4095-64del (MSH6) XP_024308587.1:n.4094+59_4095-64del
XM_024452820.1:c.3911+59_3912-64del (MSH6) XP_024308588.1:n.3911+59_3912-64del
XM_024452821.1:c.3797+59_3798-64del (MSH6) XP_024308589.1:n.3797+59_3798-64del
XM_024452822.1:c.3188+59_3189-64del (MSH6) XP_024308590.1:n.3188+59_3189-64del
NM_000179.3:c.4001+59_4002-64del (MSH6) MANE Select NP_000170.1:n.4001+59_4002-64del
NM_001281492.2:c.3611+59_3612-64del (MSH6) NP_001268421.1:n.3611+59_3612-64del
NM_001281493.2:c.3095+59_3096-64del (MSH6) NP_001268422.1:n.3095+59_3096-64del
NM_001281494.2:c.3095+59_3096-64del (MSH6) NP_001268423.1:n.3095+59_3096-64del