Canonical Allele Identifier: CA357801

Linked Data

ClinVar Variation Id: 224535
dbSNP Id: rs869312770

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47800831_47800832del , CM000664.2:g.47800831_47800832del GRCh38
NC_000002.11:g.48027970_48027971del , CM000664.1:g.48027970_48027971del GRCh37
NC_000002.10:g.47881474_47881475del NCBI36
NG_007111.1:g.22685_22686del , LRG_219:g.22685_22686del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.2551_2552del (MSH6) ENSP00000406248.2:p.Ser851ProfsTer15
ENST00000420813.6:c.2551_2552del (MSH6) ENSP00000390382.2:p.Ser851ProfsTer15
ENST00000455383.6:c.2551_2552del (MSH6) ENSP00000397484.2:p.Ser851ProfsTer15
ENST00000700004.2:c.2848_2849del (MSH6) ENSP00000514752.2:p.Ser950ProfsTer15
ENST00000699999.1:n.2932_2933del (MSH6)
ENST00000700000.1:c.1606+1242_1606+1243del (MSH6) ENSP00000514749.1:n.1606+1242_1606+1243de...
ENST00000700002.1:c.2854_2855del (MSH6) ENSP00000514750.1:p.Ser952ProfsTer15
ENST00000700003.1:c.628-2589_628-2588del (MSH6) ENSP00000514751.1:n.628-2589_628-2588del
ENST00000700004.1:c.2005_2006del (MSH6) ENSP00000514752.1:p.Ser669ProfsTer15
ENST00000234420.11:c.2848_2849del (MSH6) MANE Select ENSP00000234420.5:p.Ser950ProfsTer15
ENST00000540021.6:c.2458_2459del (MSH6) ENSP00000446475.1:p.Ser820ProfsTer15
ENST00000652107.1:c.2551_2552del (MSH6) ENSP00000498629.1:p.Ser851ProfsTer15
ENST00000673637.1:c.2551_2552del (MSH6) ENSP00000501310.1:p.Ser851ProfsTer15
ENST00000234420.9:c.2848_2849del (MSH6) ENSP00000234420.4:p.Ser950ProfsTer15
ENST00000405808.5:c.169+7365_169+7366del (FBXO11) ENSP00000385127.1:n.169+7365_169+7366del
ENST00000434234.5:c.*124+7164_*124+7165del (FBXO11) ENSP00000402692.1:n.*124+7164_*124+7165de...
ENST00000445503.5:c.*2195_*2196del (MSH6) ENSP00000405294.1:n.*2195_*2196del
ENST00000538136.1:c.1942_1943del (MSH6) ENSP00000438580.1:p.Ser648ProfsTer15
ENST00000540021.5:c.2458_2459del (MSH6) ENSP00000446475.1:p.Ser820ProfsTer15
ENST00000614496.4:c.1942_1943del (MSH6) ENSP00000477844.1:p.Ser648ProfsTer15
ENST00000616033.4:c.2845_2846del (MSH6) ENSP00000480261.1:p.Ser949ProfsTer15
ENST00000622629.4:c.-249_-248del (MSH6) ENSP00000482078.1:n.-249_-248del
NM_000179.2:c.2848_2849del , LRG_219t1:c.2848_2849del (MSH6) NP_000170.1:p.Ser950ProfsTer15
NM_001281492.1:c.2458_2459del (MSH6) NP_001268421.1:p.Ser820ProfsTer15
NM_001281493.1:c.1942_1943del (MSH6) NP_001268422.1:p.Ser648ProfsTer15
NM_001281494.1:c.1942_1943del (MSH6) NP_001268423.1:p.Ser648ProfsTer15
XM_005264271.1:c.2551_2552del (MSH6) XP_005264328.1:p.Ser851ProfsTer15
XM_011532798.1:c.2665_2666del (MSH6) XP_011531100.1:p.Ser889ProfsTer15
XM_011532799.1:c.2551_2552del (MSH6) XP_011531101.1:p.Ser851ProfsTer15
XM_011532800.1:c.2551_2552del (MSH6) XP_011531102.1:p.Ser851ProfsTer15
XM_024452819.1:c.2848_2849del (MSH6) XP_024308587.1:p.Ser950ProfsTer15
XM_024452820.1:c.2665_2666del (MSH6) XP_024308588.1:p.Ser889ProfsTer15
XM_024452821.1:c.2551_2552del (MSH6) XP_024308589.1:p.Ser851ProfsTer15
XM_024452822.1:c.1942_1943del (MSH6) XP_024308590.1:p.Ser648ProfsTer15
NM_000179.3:c.2848_2849del (MSH6) MANE Select NP_000170.1:p.Ser950ProfsTer15
NM_001281492.2:c.2458_2459del (MSH6) NP_001268421.1:p.Ser820ProfsTer15
NM_001281493.2:c.1942_1943del (MSH6) NP_001268422.1:p.Ser648ProfsTer15
NM_001281494.2:c.1942_1943del (MSH6) NP_001268423.1:p.Ser648ProfsTer15