Canonical Allele Identifier: CA769465432

Linked Data

dbSNP Id: rs1336670924

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806148_47806160del , CM000664.2:g.47806148_47806160del GRCh38
NC_000002.11:g.48033287_48033299del , CM000664.1:g.48033287_48033299del GRCh37
NC_000002.10:g.47886791_47886803del NCBI36
NG_007111.1:g.28002_28014del , LRG_219:g.28002_28014del
NG_008397.1:g.104518_104530del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3350-56_3350-44del (MSH6) ENSP00000406248.2:n.3350-56_3350-44del
ENST00000420813.6:c.3350-56_3350-44del (MSH6) ENSP00000390382.2:n.3350-56_3350-44del
ENST00000455383.6:c.3350-56_3350-44del (MSH6) ENSP00000397484.2:n.3350-56_3350-44del
ENST00000700004.2:c.3263-56_3263-44del (MSH6) ENSP00000514752.2:n.3263-56_3263-44del
ENST00000699999.1:n.4321-56_4321-44del (MSH6)
ENST00000700000.1:c.2081-56_2081-44del (MSH6) ENSP00000514749.1:n.2081-56_2081-44del
ENST00000700002.1:c.3653-56_3653-44del (MSH6) ENSP00000514750.1:n.3653-56_3653-44del
ENST00000700003.1:c.1102-56_1102-44del (MSH6) ENSP00000514751.1:n.1102-56_1102-44del
ENST00000700004.1:c.2420-56_2420-44del (MSH6) ENSP00000514752.1:n.2420-56_2420-44del
ENST00000700005.1:n.2498-56_2498-44del (MSH6)
ENST00000700006.1:n.4749_4761del (MSH6)
ENST00000700007.1:n.2242-56_2242-44del (MSH6)
ENST00000700008.1:n.1816-56_1816-44del (MSH6)
ENST00000700009.1:n.2255_2267del (MSH6)
ENST00000700010.1:n.1056-56_1056-44del (MSH6)
ENST00000700011.1:n.2941-56_2941-44del (MSH6)
ENST00000682451.1:n.4590_4602del (FBXO11)
ENST00000684712.1:n.4852_4864del (FBXO11)
ENST00000234420.11:c.3647-56_3647-44del (MSH6) MANE Select ENSP00000234420.5:n.3647-56_3647-44del
ENST00000540021.6:c.3257-56_3257-44del (MSH6) ENSP00000446475.1:n.3257-56_3257-44del
ENST00000652107.1:c.3350-56_3350-44del (MSH6) ENSP00000498629.1:n.3350-56_3350-44del
ENST00000673637.1:c.3350-56_3350-44del (MSH6) ENSP00000501310.1:n.3350-56_3350-44del
ENST00000234420.9:c.3647-56_3647-44del (MSH6) ENSP00000234420.4:n.3647-56_3647-44del
ENST00000405808.5:c.169+2037_169+2049del (FBXO11) ENSP00000385127.1:n.169+2037_169+2049del
ENST00000434234.5:c.*124+1836_*124+1848del (FBXO11) ENSP00000402692.1:n.*124+1836_*124+1848de...
ENST00000445503.5:c.*2994-56_*2994-44del (MSH6) ENSP00000405294.1:n.*2994-56_*2994-44del
ENST00000538136.1:c.2741-56_2741-44del (MSH6) ENSP00000438580.1:n.2741-56_2741-44del
ENST00000540021.5:c.3257-56_3257-44del (MSH6) ENSP00000446475.1:n.3257-56_3257-44del
ENST00000614496.4:c.2741-56_2741-44del (MSH6) ENSP00000477844.1:n.2741-56_2741-44del
ENST00000622629.4:c.551-56_551-44del (MSH6) ENSP00000482078.1:n.551-56_551-44del
NM_000179.2:c.3647-56_3647-44del , LRG_219t1:c.3647-56_3647-44del (MSH6) NP_000170.1:n.3647-56_3647-44del
NM_001281492.1:c.3257-56_3257-44del (MSH6) NP_001268421.1:n.3257-56_3257-44del
NM_001281493.1:c.2741-56_2741-44del (MSH6) NP_001268422.1:n.2741-56_2741-44del
NM_001281494.1:c.2741-56_2741-44del (MSH6) NP_001268423.1:n.2741-56_2741-44del
XM_005264271.1:c.3350-56_3350-44del (MSH6) XP_005264328.1:n.3350-56_3350-44del
XM_011532798.1:c.3464-56_3464-44del (MSH6) XP_011531100.1:n.3464-56_3464-44del
XM_011532799.1:c.3350-56_3350-44del (MSH6) XP_011531101.1:n.3350-56_3350-44del
XM_011532800.1:c.3350-56_3350-44del (MSH6) XP_011531102.1:n.3350-56_3350-44del
XM_024452819.1:c.3647-56_3647-44del (MSH6) XP_024308587.1:n.3647-56_3647-44del
XM_024452820.1:c.3464-56_3464-44del (MSH6) XP_024308588.1:n.3464-56_3464-44del
XM_024452821.1:c.3350-56_3350-44del (MSH6) XP_024308589.1:n.3350-56_3350-44del
XM_024452822.1:c.2741-56_2741-44del (MSH6) XP_024308590.1:n.2741-56_2741-44del
NM_000179.3:c.3647-56_3647-44del (MSH6) MANE Select NP_000170.1:n.3647-56_3647-44del
NM_001281492.2:c.3257-56_3257-44del (MSH6) NP_001268421.1:n.3257-56_3257-44del
NM_001281493.2:c.2741-56_2741-44del (MSH6) NP_001268422.1:n.2741-56_2741-44del
NM_001281494.2:c.2741-56_2741-44del (MSH6) NP_001268423.1:n.2741-56_2741-44del