Canonical Allele Identifier: CA2658967391

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806075_47806088del , CM000664.2:g.47806075_47806088del GRCh38
NC_000002.11:g.48033214_48033227del , CM000664.1:g.48033214_48033227del GRCh37
NC_000002.10:g.47886718_47886731del NCBI36
NG_007111.1:g.27929_27942del , LRG_219:g.27929_27942del
NG_008397.1:g.104590_104603del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3350-129_3350-116del (MSH6) ENSP00000406248.2:n.3350-129_3350-116del
ENST00000420813.6:c.3350-129_3350-116del (MSH6) ENSP00000390382.2:n.3350-129_3350-116del
ENST00000455383.6:c.3350-129_3350-116del (MSH6) ENSP00000397484.2:n.3350-129_3350-116del
ENST00000700004.2:c.3263-129_3263-116del (MSH6) ENSP00000514752.2:n.3263-129_3263-116del
ENST00000699999.1:n.4321-129_4321-116del (MSH6)
ENST00000700000.1:c.2081-129_2081-116del (MSH6) ENSP00000514749.1:n.2081-129_2081-116del
ENST00000700002.1:c.3653-129_3653-116del (MSH6) ENSP00000514750.1:n.3653-129_3653-116del
ENST00000700003.1:c.1102-129_1102-116del (MSH6) ENSP00000514751.1:n.1102-129_1102-116del
ENST00000700004.1:c.2420-129_2420-116del (MSH6) ENSP00000514752.1:n.2420-129_2420-116del
ENST00000700005.1:n.2498-129_2498-116del (MSH6)
ENST00000700006.1:n.4676_4689del (MSH6)
ENST00000700007.1:n.2242-129_2242-116del (MSH6)
ENST00000700008.1:n.1816-129_1816-116del (MSH6)
ENST00000700009.1:n.2182_2195del (MSH6)
ENST00000700010.1:n.1056-129_1056-116del (MSH6)
ENST00000700011.1:n.2941-129_2941-116del (MSH6)
ENST00000682451.1:n.4662_4675del (FBXO11)
ENST00000684712.1:n.4924_4937del (FBXO11)
ENST00000234420.11:c.3647-129_3647-116del (MSH6) MANE Select ENSP00000234420.5:n.3647-129_3647-116del
ENST00000540021.6:c.3257-129_3257-116del (MSH6) ENSP00000446475.1:n.3257-129_3257-116del
ENST00000652107.1:c.3350-129_3350-116del (MSH6) ENSP00000498629.1:n.3350-129_3350-116del
ENST00000673637.1:c.3350-129_3350-116del (MSH6) ENSP00000501310.1:n.3350-129_3350-116del
ENST00000234420.9:c.3647-129_3647-116del (MSH6) ENSP00000234420.4:n.3647-129_3647-116del
ENST00000405808.5:c.169+2109_169+2122del (FBXO11) ENSP00000385127.1:n.169+2109_169+2122del
ENST00000434234.5:c.*124+1908_*124+1921del (FBXO11) ENSP00000402692.1:n.*124+1908_*124+1921de...
ENST00000445503.5:c.*2994-129_*2994-116del (MSH6) ENSP00000405294.1:n.*2994-129_*2994-116de...
ENST00000538136.1:c.2741-129_2741-116del (MSH6) ENSP00000438580.1:n.2741-129_2741-116del
ENST00000540021.5:c.3257-129_3257-116del (MSH6) ENSP00000446475.1:n.3257-129_3257-116del
ENST00000614496.4:c.2741-129_2741-116del (MSH6) ENSP00000477844.1:n.2741-129_2741-116del
ENST00000622629.4:c.551-129_551-116del (MSH6) ENSP00000482078.1:n.551-129_551-116del
NM_000179.2:c.3647-129_3647-116del , LRG_219t1:c.3647-129_3647-116del (MSH6) NP_000170.1:n.3647-129_3647-116del
NM_001281492.1:c.3257-129_3257-116del (MSH6) NP_001268421.1:n.3257-129_3257-116del
NM_001281493.1:c.2741-129_2741-116del (MSH6) NP_001268422.1:n.2741-129_2741-116del
NM_001281494.1:c.2741-129_2741-116del (MSH6) NP_001268423.1:n.2741-129_2741-116del
XM_005264271.1:c.3350-129_3350-116del (MSH6) XP_005264328.1:n.3350-129_3350-116del
XM_011532798.1:c.3464-129_3464-116del (MSH6) XP_011531100.1:n.3464-129_3464-116del
XM_011532799.1:c.3350-129_3350-116del (MSH6) XP_011531101.1:n.3350-129_3350-116del
XM_011532800.1:c.3350-129_3350-116del (MSH6) XP_011531102.1:n.3350-129_3350-116del
XM_024452819.1:c.3647-129_3647-116del (MSH6) XP_024308587.1:n.3647-129_3647-116del
XM_024452820.1:c.3464-129_3464-116del (MSH6) XP_024308588.1:n.3464-129_3464-116del
XM_024452821.1:c.3350-129_3350-116del (MSH6) XP_024308589.1:n.3350-129_3350-116del
XM_024452822.1:c.2741-129_2741-116del (MSH6) XP_024308590.1:n.2741-129_2741-116del
NM_000179.3:c.3647-129_3647-116del (MSH6) MANE Select NP_000170.1:n.3647-129_3647-116del
NM_001281492.2:c.3257-129_3257-116del (MSH6) NP_001268421.1:n.3257-129_3257-116del
NM_001281493.2:c.2741-129_2741-116del (MSH6) NP_001268422.1:n.2741-129_2741-116del
NM_001281494.2:c.2741-129_2741-116del (MSH6) NP_001268423.1:n.2741-129_2741-116del