Canonical Allele Identifier: CA2496049403

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47800193_47800204delinsCAGTGACATTAA , CM000664.2:g.47800193_47800204delinsCAGTGACATTAA GRCh38
NC_000002.11:g.48027332_48027343delinsCAGTGACATTAA , CM000664.1:g.48027332_48027343delinsCAGTGACATTAA GRCh37
NC_000002.10:g.47880836_47880847delinsCAGTGACATTAA NCBI36
NG_007111.1:g.22047_22058delinsCAGTGACATTAA , LRG_219:g.22047_22058delinsCAGTGACATTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.1913_1924delinsCAGTGACATTAA (MSH6) ENSP00000406248.2:p.Ala638=
ENST00000420813.6:c.1913_1924delinsCAGTGACATTAA (MSH6) ENSP00000390382.2:p.Ala638=
ENST00000455383.6:c.1913_1924delinsCAGTGACATTAA (MSH6) ENSP00000397484.2:p.Ala638=
ENST00000700004.2:c.2210_2221delinsCAGTGACATTAA (MSH6) ENSP00000514752.2:p.Ala737=
ENST00000699999.1:n.2294_2305delinsCAGTGACATTAA (MSH6)
ENST00000700000.1:c.1606+604_1606+615delinsCAGTGACATTAA (MSH6) ENSP00000514749.1:n.1606+604_1606+615delinsCAGTGACATTAA
ENST00000700002.1:c.2216_2227delinsCAGTGACATTAA (MSH6) ENSP00000514750.1:p.Ala739=
ENST00000700003.1:c.628-3227_628-3216delinsCAGTGACATTAA (MSH6) ENSP00000514751.1:n.628-3227_628-3216delinsCAGTGACATTAA
ENST00000700004.1:c.1367_1378delinsCAGTGACATTAA (MSH6) ENSP00000514752.1:p.Ala456=
ENST00000234420.11:c.2210_2221delinsCAGTGACATTAA (MSH6) MANE Select ENSP00000234420.5:p.Ala737=
ENST00000540021.6:c.1820_1831delinsCAGTGACATTAA (MSH6) ENSP00000446475.1:p.Ala607=
ENST00000652107.1:c.1913_1924delinsCAGTGACATTAA (MSH6) ENSP00000498629.1:p.Ala638=
ENST00000673637.1:c.1913_1924delinsCAGTGACATTAA (MSH6) ENSP00000501310.1:p.Ala638=
ENST00000234420.9:c.2210_2221delinsCAGTGACATTAA (MSH6) ENSP00000234420.4:p.Ala737=
ENST00000405808.5:c.169+7991_169+8002delinsTTAATGTCACTG (FBXO11) ENSP00000385127.1:n.169+7991_169+8002delinsTTAATGTCACTG
ENST00000434234.5:c.*124+7790_*124+7801delinsTTAATGTCACTG (FBXO11) ENSP00000402692.1:n.*124+7790_*124+7801delinsTTAATGTCACTG
ENST00000445503.5:c.*1557_*1568delinsCAGTGACATTAA (MSH6) ENSP00000405294.1:n.*1557_*1568delinsCAGTGACATTAA
ENST00000538136.1:c.1304_1315delinsCAGTGACATTAA (MSH6) ENSP00000438580.1:p.Ala435=
ENST00000540021.5:c.1820_1831delinsCAGTGACATTAA (MSH6) ENSP00000446475.1:p.Ala607=
ENST00000614496.4:c.1304_1315delinsCAGTGACATTAA (MSH6) ENSP00000477844.1:p.Ala435=
ENST00000616033.4:c.2207_2218delinsCAGTGACATTAA (MSH6) ENSP00000480261.1:p.Ala736=
ENST00000622629.4:c.-887_-876delinsCAGTGACATTAA (MSH6) ENSP00000482078.1:n.-887_-876delinsCAGTGACATTAA
NM_000179.2:c.2210_2221delinsCAGTGACATTAA , LRG_219t1:c.2210_2221delinsCAGTGACATTAA (MSH6) NP_000170.1:p.Ala737=
NM_001281492.1:c.1820_1831delinsCAGTGACATTAA (MSH6) NP_001268421.1:p.Ala607=
NM_001281493.1:c.1304_1315delinsCAGTGACATTAA (MSH6) NP_001268422.1:p.Ala435=
NM_001281494.1:c.1304_1315delinsCAGTGACATTAA (MSH6) NP_001268423.1:p.Ala435=
XM_005264271.1:c.1913_1924delinsCAGTGACATTAA (MSH6) XP_005264328.1:p.Ala638=
XM_011532798.1:c.2027_2038delinsCAGTGACATTAA (MSH6) XP_011531100.1:p.Ala676=
XM_011532799.1:c.1913_1924delinsCAGTGACATTAA (MSH6) XP_011531101.1:p.Ala638=
XM_011532800.1:c.1913_1924delinsCAGTGACATTAA (MSH6) XP_011531102.1:p.Ala638=
XM_024452819.1:c.2210_2221delinsCAGTGACATTAA (MSH6) XP_024308587.1:p.Ala737=
XM_024452820.1:c.2027_2038delinsCAGTGACATTAA (MSH6) XP_024308588.1:p.Ala676=
XM_024452821.1:c.1913_1924delinsCAGTGACATTAA (MSH6) XP_024308589.1:p.Ala638=
XM_024452822.1:c.1304_1315delinsCAGTGACATTAA (MSH6) XP_024308590.1:p.Ala435=
NM_000179.3:c.2210_2221delinsCAGTGACATTAA (MSH6) MANE Select NP_000170.1:p.Ala737=
NM_001281492.2:c.1820_1831delinsCAGTGACATTAA (MSH6) NP_001268421.1:p.Ala607=
NM_001281493.2:c.1304_1315delinsCAGTGACATTAA (MSH6) NP_001268422.1:p.Ala435=
NM_001281494.2:c.1304_1315delinsCAGTGACATTAA (MSH6) NP_001268423.1:p.Ala435=