Canonical Allele Identifier: CA2496048272

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47798913_47798919delinsTAAAAGG , CM000664.2:g.47798913_47798919delinsTAAAAGG GRCh38
NC_000002.11:g.48026052_48026058delinsTAAAAGG , CM000664.1:g.48026052_48026058delinsTAAAAGG GRCh37
NC_000002.10:g.47879556_47879562delinsTAAAAGG NCBI36
NG_007111.1:g.20767_20773delinsTAAAAGG , LRG_219:g.20767_20773delinsTAAAAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.633_639delinsTAAAAGG (MSH6) ENSP00000406248.2:p.Leu211=
ENST00000420813.6:c.633_639delinsTAAAAGG (MSH6) ENSP00000390382.2:p.Leu211=
ENST00000455383.6:c.633_639delinsTAAAAGG (MSH6) ENSP00000397484.2:p.Leu211=
ENST00000700004.2:c.930_936delinsTAAAAGG (MSH6) ENSP00000514752.2:p.Leu310=
ENST00000699999.1:n.1014_1020delinsTAAAAGG (MSH6)
ENST00000700000.1:c.930_936delinsTAAAAGG (MSH6) ENSP00000514749.1:p.Leu310=
ENST00000700002.1:c.936_942delinsTAAAAGG (MSH6) ENSP00000514750.1:p.Leu312=
ENST00000700003.1:c.627+2850_627+2856delinsTAAAAGG (MSH6) ENSP00000514751.1:n.627+2850_627+2856deli...
ENST00000700004.1:c.87_93delinsTAAAAGG (MSH6) ENSP00000514752.1:p.Leu29=
ENST00000234420.11:c.930_936delinsTAAAAGG (MSH6) MANE Select ENSP00000234420.5:p.Leu310=
ENST00000540021.6:c.540_546delinsTAAAAGG (MSH6) ENSP00000446475.1:p.Leu180=
ENST00000652107.1:c.633_639delinsTAAAAGG (MSH6) ENSP00000498629.1:p.Leu211=
ENST00000673637.1:c.633_639delinsTAAAAGG (MSH6) ENSP00000501310.1:p.Leu211=
ENST00000234420.9:c.930_936delinsTAAAAGG (MSH6) ENSP00000234420.4:p.Leu310=
ENST00000405808.5:c.169+9276_169+9282delinsCCTTTTA (FBXO11) ENSP00000385127.1:n.169+9276_169+9282deli...
ENST00000434234.5:c.*124+9075_*124+9081delinsCCTTTTA (FBXO11) ENSP00000402692.1:n.*124+9075_*124+9081de...
ENST00000445503.5:c.*277_*283delinsTAAAAGG (MSH6) ENSP00000405294.1:n.*277_*283delinsTAAAAG...
ENST00000456246.1:c.*418_*424delinsTAAAAGG (MSH6) ENSP00000410570.1:n.*418_*424delinsTAAAAG...
ENST00000538136.1:c.24_30delinsTAAAAGG (MSH6) ENSP00000438580.1:p.Leu8=
ENST00000540021.5:c.540_546delinsTAAAAGG (MSH6) ENSP00000446475.1:p.Leu180=
ENST00000614496.4:c.24_30delinsTAAAAGG (MSH6) ENSP00000477844.1:p.Leu8=
ENST00000616033.4:c.927_933delinsTAAAAGG (MSH6) ENSP00000480261.1:p.Leu309=
ENST00000622629.4:c.-2167_-2161delinsTAAAAGG (MSH6) ENSP00000482078.1:n.-2167_-2161delinsTAAA...
NM_000179.2:c.930_936delinsTAAAAGG , LRG_219t1:c.930_936delinsTAAAAGG (MSH6) NP_000170.1:p.Leu310=
NM_001281492.1:c.540_546delinsTAAAAGG (MSH6) NP_001268421.1:p.Leu180=
NM_001281493.1:c.24_30delinsTAAAAGG (MSH6) NP_001268422.1:p.Leu8=
NM_001281494.1:c.24_30delinsTAAAAGG (MSH6) NP_001268423.1:p.Leu8=
XM_005264271.1:c.633_639delinsTAAAAGG (MSH6) XP_005264328.1:p.Leu211=
XM_011532798.1:c.747_753delinsTAAAAGG (MSH6) XP_011531100.1:p.Leu249=
XM_011532799.1:c.633_639delinsTAAAAGG (MSH6) XP_011531101.1:p.Leu211=
XM_011532800.1:c.633_639delinsTAAAAGG (MSH6) XP_011531102.1:p.Leu211=
XM_024452819.1:c.930_936delinsTAAAAGG (MSH6) XP_024308587.1:p.Leu310=
XM_024452820.1:c.747_753delinsTAAAAGG (MSH6) XP_024308588.1:p.Leu249=
XM_024452821.1:c.633_639delinsTAAAAGG (MSH6) XP_024308589.1:p.Leu211=
XM_024452822.1:c.24_30delinsTAAAAGG (MSH6) XP_024308590.1:p.Leu8=
NM_000179.3:c.930_936delinsTAAAAGG (MSH6) MANE Select NP_000170.1:p.Leu310=
NM_001281492.2:c.540_546delinsTAAAAGG (MSH6) NP_001268421.1:p.Leu180=
NM_001281493.2:c.24_30delinsTAAAAGG (MSH6) NP_001268422.1:p.Leu8=
NM_001281494.2:c.24_30delinsTAAAAGG (MSH6) NP_001268423.1:p.Leu8=