Canonical Allele Identifier: CA2496048728

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799471_47799473delinsTAG , CM000664.2:g.47799471_47799473delinsTAG GRCh38
NC_000002.11:g.48026610_48026612delinsTAG , CM000664.1:g.48026610_48026612delinsTAG GRCh37
NC_000002.10:g.47880114_47880116delinsTAG NCBI36
NG_007111.1:g.21325_21327delinsTAG , LRG_219:g.21325_21327delinsTAG

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.1191_1193delinsTAG (MSH6) ENSP00000406248.2:p.Cys397=
ENST00000420813.6:c.1191_1193delinsTAG (MSH6) ENSP00000390382.2:p.Cys397=
ENST00000455383.6:c.1191_1193delinsTAG (MSH6) ENSP00000397484.2:p.Cys397=
ENST00000700004.2:c.1488_1490delinsTAG (MSH6) ENSP00000514752.2:p.Cys496=
ENST00000699999.1:n.1572_1574delinsTAG (MSH6)
ENST00000700000.1:c.1488_1490delinsTAG (MSH6) ENSP00000514749.1:p.Cys496=
ENST00000700002.1:c.1494_1496delinsTAG (MSH6) ENSP00000514750.1:p.Cys498=
ENST00000700003.1:c.627+3408_627+3410delinsTAG (MSH6) ENSP00000514751.1:n.627+3408_627+3410deli...
ENST00000700004.1:c.645_647delinsTAG (MSH6) ENSP00000514752.1:p.Cys215=
ENST00000234420.11:c.1488_1490delinsTAG (MSH6) MANE Select ENSP00000234420.5:p.Cys496=
ENST00000540021.6:c.1098_1100delinsTAG (MSH6) ENSP00000446475.1:p.Cys366=
ENST00000652107.1:c.1191_1193delinsTAG (MSH6) ENSP00000498629.1:p.Cys397=
ENST00000673637.1:c.1191_1193delinsTAG (MSH6) ENSP00000501310.1:p.Cys397=
ENST00000234420.9:c.1488_1490delinsTAG (MSH6) ENSP00000234420.4:p.Cys496=
ENST00000405808.5:c.169+8722_169+8724delinsCTA (FBXO11) ENSP00000385127.1:n.169+8722_169+8724deli...
ENST00000434234.5:c.*124+8521_*124+8523delinsCTA (FBXO11) ENSP00000402692.1:n.*124+8521_*124+8523de...
ENST00000445503.5:c.*835_*837delinsTAG (MSH6) ENSP00000405294.1:n.*835_*837delinsTAG
ENST00000538136.1:c.582_584delinsTAG (MSH6) ENSP00000438580.1:p.Cys194=
ENST00000540021.5:c.1098_1100delinsTAG (MSH6) ENSP00000446475.1:p.Cys366=
ENST00000614496.4:c.582_584delinsTAG (MSH6) ENSP00000477844.1:p.Cys194=
ENST00000616033.4:c.1485_1487delinsTAG (MSH6) ENSP00000480261.1:p.Cys495=
ENST00000622629.4:c.-1609_-1607delinsTAG (MSH6) ENSP00000482078.1:n.-1609_-1607delinsTAG
NM_000179.2:c.1488_1490delinsTAG , LRG_219t1:c.1488_1490delinsTAG (MSH6) NP_000170.1:p.Cys496=
NM_001281492.1:c.1098_1100delinsTAG (MSH6) NP_001268421.1:p.Cys366=
NM_001281493.1:c.582_584delinsTAG (MSH6) NP_001268422.1:p.Cys194=
NM_001281494.1:c.582_584delinsTAG (MSH6) NP_001268423.1:p.Cys194=
XM_005264271.1:c.1191_1193delinsTAG (MSH6) XP_005264328.1:p.Cys397=
XM_011532798.1:c.1305_1307delinsTAG (MSH6) XP_011531100.1:p.Cys435=
XM_011532799.1:c.1191_1193delinsTAG (MSH6) XP_011531101.1:p.Cys397=
XM_011532800.1:c.1191_1193delinsTAG (MSH6) XP_011531102.1:p.Cys397=
XM_024452819.1:c.1488_1490delinsTAG (MSH6) XP_024308587.1:p.Cys496=
XM_024452820.1:c.1305_1307delinsTAG (MSH6) XP_024308588.1:p.Cys435=
XM_024452821.1:c.1191_1193delinsTAG (MSH6) XP_024308589.1:p.Cys397=
XM_024452822.1:c.582_584delinsTAG (MSH6) XP_024308590.1:p.Cys194=
NM_000179.3:c.1488_1490delinsTAG (MSH6) MANE Select NP_000170.1:p.Cys496=
NM_001281492.2:c.1098_1100delinsTAG (MSH6) NP_001268421.1:p.Cys366=
NM_001281493.2:c.582_584delinsTAG (MSH6) NP_001268422.1:p.Cys194=
NM_001281494.2:c.582_584delinsTAG (MSH6) NP_001268423.1:p.Cys194=