Canonical Allele Identifier: CA16617663

Linked Data

ClinVar Variation Id: 419665
ClinVar RCV Id: RCV000481527
dbSNP Id: rs1064794028

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799981_47799982del , CM000664.2:g.47799981_47799982del GRCh38
NC_000002.11:g.48027120_48027121del , CM000664.1:g.48027120_48027121del GRCh37
NC_000002.10:g.47880624_47880625del NCBI36
NG_007111.1:g.21835_21836del , LRG_219:g.21835_21836del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.1701_1702del (MSH6) ENSP00000406248.2:p.Asp568PhefsTer11
ENST00000420813.6:c.1701_1702del (MSH6) ENSP00000390382.2:p.Asp568PhefsTer11
ENST00000455383.6:c.1701_1702del (MSH6) ENSP00000397484.2:p.Asp568PhefsTer11
ENST00000700004.2:c.1998_1999del (MSH6) ENSP00000514752.2:p.Asp667PhefsTer11
ENST00000699999.1:n.2082_2083del (MSH6)
ENST00000700000.1:c.1606+392_1606+393del (MSH6) ENSP00000514749.1:n.1606+392_1606+393del
ENST00000700002.1:c.2004_2005del (MSH6) ENSP00000514750.1:p.Asp669PhefsTer11
ENST00000700003.1:c.628-3439_628-3438del (MSH6) ENSP00000514751.1:n.628-3439_628-3438del
ENST00000700004.1:c.1155_1156del (MSH6) ENSP00000514752.1:p.Asp386PhefsTer11
ENST00000234420.11:c.1998_1999del (MSH6) MANE Select ENSP00000234420.5:p.Asp667PhefsTer11
ENST00000540021.6:c.1608_1609del (MSH6) ENSP00000446475.1:p.Asp537PhefsTer11
ENST00000652107.1:c.1701_1702del (MSH6) ENSP00000498629.1:p.Asp568PhefsTer11
ENST00000673637.1:c.1701_1702del (MSH6) ENSP00000501310.1:p.Asp568PhefsTer11
ENST00000234420.9:c.1998_1999del (MSH6) ENSP00000234420.4:p.Asp667PhefsTer11
ENST00000405808.5:c.169+8213_169+8214del (FBXO11) ENSP00000385127.1:n.169+8213_169+8214del
ENST00000434234.5:c.*124+8012_*124+8013del (FBXO11) ENSP00000402692.1:n.*124+8012_*124+8013de...
ENST00000445503.5:c.*1345_*1346del (MSH6) ENSP00000405294.1:n.*1345_*1346del
ENST00000538136.1:c.1092_1093del (MSH6) ENSP00000438580.1:p.Asp365PhefsTer11
ENST00000540021.5:c.1608_1609del (MSH6) ENSP00000446475.1:p.Asp537PhefsTer11
ENST00000614496.4:c.1092_1093del (MSH6) ENSP00000477844.1:p.Asp365PhefsTer11
ENST00000616033.4:c.1995_1996del (MSH6) ENSP00000480261.1:p.Asp666PhefsTer11
ENST00000622629.4:c.-1099_-1098del (MSH6) ENSP00000482078.1:n.-1099_-1098del
NM_000179.2:c.1998_1999del , LRG_219t1:c.1998_1999del (MSH6) NP_000170.1:p.Asp667PhefsTer11
NM_001281492.1:c.1608_1609del (MSH6) NP_001268421.1:p.Asp537PhefsTer11
NM_001281493.1:c.1092_1093del (MSH6) NP_001268422.1:p.Asp365PhefsTer11
NM_001281494.1:c.1092_1093del (MSH6) NP_001268423.1:p.Asp365PhefsTer11
XM_005264271.1:c.1701_1702del (MSH6) XP_005264328.1:p.Asp568PhefsTer11
XM_011532798.1:c.1815_1816del (MSH6) XP_011531100.1:p.Asp606PhefsTer11
XM_011532799.1:c.1701_1702del (MSH6) XP_011531101.1:p.Asp568PhefsTer11
XM_011532800.1:c.1701_1702del (MSH6) XP_011531102.1:p.Asp568PhefsTer11
XM_024452819.1:c.1998_1999del (MSH6) XP_024308587.1:p.Asp667PhefsTer11
XM_024452820.1:c.1815_1816del (MSH6) XP_024308588.1:p.Asp606PhefsTer11
XM_024452821.1:c.1701_1702del (MSH6) XP_024308589.1:p.Asp568PhefsTer11
XM_024452822.1:c.1092_1093del (MSH6) XP_024308590.1:p.Asp365PhefsTer11
NM_000179.3:c.1998_1999del (MSH6) MANE Select NP_000170.1:p.Asp667PhefsTer11
NM_001281492.2:c.1608_1609del (MSH6) NP_001268421.1:p.Asp537PhefsTer11
NM_001281493.2:c.1092_1093del (MSH6) NP_001268422.1:p.Asp365PhefsTer11
NM_001281494.2:c.1092_1093del (MSH6) NP_001268423.1:p.Asp365PhefsTer11