Canonical Allele Identifier: CA2496048223

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47798860_47798866delinsCCTGTCA , CM000664.2:g.47798860_47798866delinsCCTGTCA GRCh38
NC_000002.11:g.48025999_48026005delinsCCTGTCA , CM000664.1:g.48025999_48026005delinsCCTGTCA GRCh37
NC_000002.10:g.47879503_47879509delinsCCTGTCA NCBI36
NG_007111.1:g.20714_20720delinsCCTGTCA , LRG_219:g.20714_20720delinsCCTGTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.580_586delinsCCTGTCA (MSH6) ENSP00000406248.2:p.Pro194=
ENST00000420813.6:c.580_586delinsCCTGTCA (MSH6) ENSP00000390382.2:p.Pro194=
ENST00000455383.6:c.580_586delinsCCTGTCA (MSH6) ENSP00000397484.2:p.Pro194=
ENST00000700004.2:c.877_883delinsCCTGTCA (MSH6) ENSP00000514752.2:p.Pro293=
ENST00000699999.1:n.961_967delinsCCTGTCA (MSH6)
ENST00000700000.1:c.877_883delinsCCTGTCA (MSH6) ENSP00000514749.1:p.Pro293=
ENST00000700002.1:c.883_889delinsCCTGTCA (MSH6) ENSP00000514750.1:p.Pro295=
ENST00000700003.1:c.627+2797_627+2803delinsCCTGTCA (MSH6) ENSP00000514751.1:n.627+2797_627+2803delinsCCTGTCA
ENST00000700004.1:c.34_40delinsCCTGTCA (MSH6) ENSP00000514752.1:p.Pro12=
ENST00000234420.11:c.877_883delinsCCTGTCA (MSH6) MANE Select ENSP00000234420.5:p.Pro293=
ENST00000540021.6:c.487_493delinsCCTGTCA (MSH6) ENSP00000446475.1:p.Pro163=
ENST00000652107.1:c.580_586delinsCCTGTCA (MSH6) ENSP00000498629.1:p.Pro194=
ENST00000673637.1:c.580_586delinsCCTGTCA (MSH6) ENSP00000501310.1:p.Pro194=
ENST00000234420.9:c.877_883delinsCCTGTCA (MSH6) ENSP00000234420.4:p.Pro293=
ENST00000405808.5:c.169+9329_169+9335delinsTGACAGG (FBXO11) ENSP00000385127.1:n.169+9329_169+9335delinsTGACAGG
ENST00000434234.5:c.*124+9128_*124+9134delinsTGACAGG (FBXO11) ENSP00000402692.1:n.*124+9128_*124+9134delinsTGACAGG
ENST00000445503.5:c.*224_*230delinsCCTGTCA (MSH6) ENSP00000405294.1:n.*224_*230delinsCCTGTCA
ENST00000456246.1:c.*365_*371delinsCCTGTCA (MSH6) ENSP00000410570.1:n.*365_*371delinsCCTGTCA
ENST00000538136.1:c.-30_-24delinsCCTGTCA (MSH6) ENSP00000438580.1:n.-30_-24delinsCCTGTCA
ENST00000540021.5:c.487_493delinsCCTGTCA (MSH6) ENSP00000446475.1:p.Pro163=
ENST00000614496.4:c.-30_-24delinsCCTGTCA (MSH6) ENSP00000477844.1:n.-30_-24delinsCCTGTCA
ENST00000616033.4:c.874_880delinsCCTGTCA (MSH6) ENSP00000480261.1:p.Pro292=
ENST00000622629.4:c.-2220_-2214delinsCCTGTCA (MSH6) ENSP00000482078.1:n.-2220_-2214delinsCCTGTCA
NM_000179.2:c.877_883delinsCCTGTCA , LRG_219t1:c.877_883delinsCCTGTCA (MSH6) NP_000170.1:p.Pro293=
NM_001281492.1:c.487_493delinsCCTGTCA (MSH6) NP_001268421.1:p.Pro163=
NM_001281493.1:c.-30_-24delinsCCTGTCA (MSH6) NP_001268422.1:n.-30_-24delinsCCTGTCA
NM_001281494.1:c.-30_-24delinsCCTGTCA (MSH6) NP_001268423.1:n.-30_-24delinsCCTGTCA
XM_005264271.1:c.580_586delinsCCTGTCA (MSH6) XP_005264328.1:p.Pro194=
XM_011532798.1:c.694_700delinsCCTGTCA (MSH6) XP_011531100.1:p.Pro232=
XM_011532799.1:c.580_586delinsCCTGTCA (MSH6) XP_011531101.1:p.Pro194=
XM_011532800.1:c.580_586delinsCCTGTCA (MSH6) XP_011531102.1:p.Pro194=
XM_024452819.1:c.877_883delinsCCTGTCA (MSH6) XP_024308587.1:p.Pro293=
XM_024452820.1:c.694_700delinsCCTGTCA (MSH6) XP_024308588.1:p.Pro232=
XM_024452821.1:c.580_586delinsCCTGTCA (MSH6) XP_024308589.1:p.Pro194=
XM_024452822.1:c.-30_-24delinsCCTGTCA (MSH6) XP_024308590.1:n.-30_-24delinsCCTGTCA
NM_000179.3:c.877_883delinsCCTGTCA (MSH6) MANE Select NP_000170.1:p.Pro293=
NM_001281492.2:c.487_493delinsCCTGTCA (MSH6) NP_001268421.1:p.Pro163=
NM_001281493.2:c.-30_-24delinsCCTGTCA (MSH6) NP_001268422.1:n.-30_-24delinsCCTGTCA
NM_001281494.2:c.-30_-24delinsCCTGTCA (MSH6) NP_001268423.1:n.-30_-24delinsCCTGTCA