Canonical Allele Identifier: CA2496054206

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806525_47806538delinsGAGCTTGTCCTAAA , CM000664.2:g.47806525_47806538delinsGAGCTTGTCCTAAA GRCh38
NC_000002.11:g.48033664_48033677delinsGAGCTTGTCCTAAA , CM000664.1:g.48033664_48033677delinsGAGCTTGTCCTAAA GRCh37
NC_000002.10:g.47887168_47887181delinsGAGCTTGTCCTAAA NCBI36
NG_007111.1:g.28379_28392delinsGAGCTTGTCCTAAA , LRG_219:g.28379_28392delinsGAGCTTGTCCTAAA
NG_008397.1:g.104138_104151delinsTTTAGGACAAGCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3578_3591delinsGAGCTTGTCCTAAA (MSH6) ENSP00000406248.2:p.Gly1193=
ENST00000420813.6:c.3578_3591delinsGAGCTTGTCCTAAA (MSH6) ENSP00000390382.2:p.Gly1193=
ENST00000455383.6:c.3578_3591delinsGAGCTTGTCCTAAA (MSH6) ENSP00000397484.2:p.Gly1193=
ENST00000700004.2:c.3491_3504delinsGAGCTTGTCCTAAA (MSH6) ENSP00000514752.2:p.Gly1164=
ENST00000699999.1:n.4549_4562delinsGAGCTTGTCCTAAA (MSH6)
ENST00000700000.1:c.2309_2322delinsGAGCTTGTCCTAAA (MSH6) ENSP00000514749.1:p.Gly770=
ENST00000700002.1:c.3881_3894delinsGAGCTTGTCCTAAA (MSH6) ENSP00000514750.1:p.Gly1294=
ENST00000700003.1:c.1330_1343delinsGAGCTTGTCCTAAA (MSH6) ENSP00000514751.1:n.1330_1343delinsGAGCTT...
ENST00000700004.1:c.2648_2661delinsGAGCTTGTCCTAAA (MSH6) ENSP00000514752.1:p.Gly883=
ENST00000700005.1:n.2726_2739delinsGAGCTTGTCCTAAA (MSH6)
ENST00000700006.1:n.5033_5046delinsGAGCTTGTCCTAAA (MSH6)
ENST00000700007.1:n.2470_2483delinsGAGCTTGTCCTAAA (MSH6)
ENST00000700008.1:n.2137_2150delinsGAGCTTGTCCTAAA (MSH6)
ENST00000700009.1:n.2539_2552delinsGAGCTTGTCCTAAA (MSH6)
ENST00000700010.1:n.1284_1297delinsGAGCTTGTCCTAAA (MSH6)
ENST00000700011.1:n.3169_3182delinsGAGCTTGTCCTAAA (MSH6)
ENST00000682451.1:n.4210_4223delinsTTTAGGACAAGCTC (FBXO11)
ENST00000684712.1:n.4472_4485delinsTTTAGGACAAGCTC (FBXO11)
ENST00000234420.11:c.3875_3888delinsGAGCTTGTCCTAAA (MSH6) MANE Select ENSP00000234420.5:p.Gly1292=
ENST00000540021.6:c.3485_3498delinsGAGCTTGTCCTAAA (MSH6) ENSP00000446475.1:p.Gly1162=
ENST00000652107.1:c.3578_3591delinsGAGCTTGTCCTAAA (MSH6) ENSP00000498629.1:p.Gly1193=
ENST00000673637.1:c.3578_3591delinsGAGCTTGTCCTAAA (MSH6) ENSP00000501310.1:p.Gly1193=
ENST00000234420.9:c.3875_3888delinsGAGCTTGTCCTAAA (MSH6) ENSP00000234420.4:p.Gly1292=
ENST00000405808.5:c.169+1657_169+1670delinsTTTAGGACAAGCTC (FBXO11) ENSP00000385127.1:n.169+1657_169+1670deli...
ENST00000434234.5:c.*124+1456_*124+1469delinsTTTAGGACAAGCTC (FBXO11) ENSP00000402692.1:n.*124+1456_*124+1469de...
ENST00000445503.5:c.*3222_*3235delinsGAGCTTGTCCTAAA (MSH6) ENSP00000405294.1:n.*3222_*3235delinsGAGC...
ENST00000538136.1:c.2969_2982delinsGAGCTTGTCCTAAA (MSH6) ENSP00000438580.1:p.Gly990=
ENST00000540021.5:c.3485_3498delinsGAGCTTGTCCTAAA (MSH6) ENSP00000446475.1:p.Gly1162=
ENST00000614496.4:c.2969_2982delinsGAGCTTGTCCTAAA (MSH6) ENSP00000477844.1:p.Gly990=
ENST00000622629.4:c.776_789delinsGAGCTTGTCCTAAA (MSH6) ENSP00000482078.1:p.Gly259=
NM_000179.2:c.3875_3888delinsGAGCTTGTCCTAAA , LRG_219t1:c.3875_3888delinsGAGCTTGTCCTAAA (MSH6) NP_000170.1:p.Gly1292=
NM_001281492.1:c.3485_3498delinsGAGCTTGTCCTAAA (MSH6) NP_001268421.1:p.Gly1162=
NM_001281493.1:c.2969_2982delinsGAGCTTGTCCTAAA (MSH6) NP_001268422.1:p.Gly990=
NM_001281494.1:c.2969_2982delinsGAGCTTGTCCTAAA (MSH6) NP_001268423.1:p.Gly990=
XM_005264271.1:c.3578_3591delinsGAGCTTGTCCTAAA (MSH6) XP_005264328.1:p.Gly1193=
XM_011532798.1:c.3692_3705delinsGAGCTTGTCCTAAA (MSH6) XP_011531100.1:p.Gly1231=
XM_011532799.1:c.3578_3591delinsGAGCTTGTCCTAAA (MSH6) XP_011531101.1:p.Gly1193=
XM_011532800.1:c.3578_3591delinsGAGCTTGTCCTAAA (MSH6) XP_011531102.1:p.Gly1193=
XM_024452819.1:c.3968_3981delinsGAGCTTGTCCTAAA (MSH6) XP_024308587.1:p.Gly1323=
XM_024452820.1:c.3785_3798delinsGAGCTTGTCCTAAA (MSH6) XP_024308588.1:p.Gly1262=
XM_024452821.1:c.3671_3684delinsGAGCTTGTCCTAAA (MSH6) XP_024308589.1:p.Gly1224=
XM_024452822.1:c.3062_3075delinsGAGCTTGTCCTAAA (MSH6) XP_024308590.1:p.Gly1021=
NM_000179.3:c.3875_3888delinsGAGCTTGTCCTAAA (MSH6) MANE Select NP_000170.1:p.Gly1292=
NM_001281492.2:c.3485_3498delinsGAGCTTGTCCTAAA (MSH6) NP_001268421.1:p.Gly1162=
NM_001281493.2:c.2969_2982delinsGAGCTTGTCCTAAA (MSH6) NP_001268422.1:p.Gly990=
NM_001281494.2:c.2969_2982delinsGAGCTTGTCCTAAA (MSH6) NP_001268423.1:p.Gly990=