Canonical Allele Identifier: CA2496054267

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806550_47806562delinsTAATGCAGCAAGG , CM000664.2:g.47806550_47806562delinsTAATGCAGCAAGG GRCh38
NC_000002.11:g.48033689_48033701delinsTAATGCAGCAAGG , CM000664.1:g.48033689_48033701delinsTAATGCAGCAAGG GRCh37
NC_000002.10:g.47887193_47887205delinsTAATGCAGCAAGG NCBI36
NG_007111.1:g.28404_28416delinsTAATGCAGCAAGG , LRG_219:g.28404_28416delinsTAATGCAGCAAGG
NG_008397.1:g.104114_104126delinsCCTTGCTGCATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3603_3615delinsTAATGCAGCAAGG (MSH6) ENSP00000406248.2:p.Phe1201=
ENST00000420813.6:c.3603_3615delinsTAATGCAGCAAGG (MSH6) ENSP00000390382.2:p.Phe1201=
ENST00000455383.6:c.3603_3615delinsTAATGCAGCAAGG (MSH6) ENSP00000397484.2:p.Phe1201=
ENST00000700004.2:c.3516_3528delinsTAATGCAGCAAGG (MSH6) ENSP00000514752.2:p.Phe1172=
ENST00000699999.1:n.4574_4586delinsTAATGCAGCAAGG (MSH6)
ENST00000700000.1:c.2334_2346delinsTAATGCAGCAAGG (MSH6) ENSP00000514749.1:p.Phe778=
ENST00000700002.1:c.3906_3918delinsTAATGCAGCAAGG (MSH6) ENSP00000514750.1:p.Phe1302=
ENST00000700003.1:c.1355_1367delinsTAATGCAGCAAGG (MSH6) ENSP00000514751.1:n.1355_1367delinsTAATGCAGCAAGG
ENST00000700004.1:c.2673_2685delinsTAATGCAGCAAGG (MSH6) ENSP00000514752.1:p.Phe891=
ENST00000700005.1:n.2751_2763delinsTAATGCAGCAAGG (MSH6)
ENST00000700006.1:n.5058_5070delinsTAATGCAGCAAGG (MSH6)
ENST00000700007.1:n.2495_2507delinsTAATGCAGCAAGG (MSH6)
ENST00000700008.1:n.2162_2174delinsTAATGCAGCAAGG (MSH6)
ENST00000700009.1:n.2564_2576delinsTAATGCAGCAAGG (MSH6)
ENST00000700010.1:n.1309_1321delinsTAATGCAGCAAGG (MSH6)
ENST00000700011.1:n.3194_3206delinsTAATGCAGCAAGG (MSH6)
ENST00000682451.1:n.4186_4198delinsCCTTGCTGCATTA (FBXO11)
ENST00000684712.1:n.4448_4460delinsCCTTGCTGCATTA (FBXO11)
ENST00000234420.11:c.3900_3912delinsTAATGCAGCAAGG (MSH6) MANE Select ENSP00000234420.5:p.Phe1300=
ENST00000540021.6:c.3510_3522delinsTAATGCAGCAAGG (MSH6) ENSP00000446475.1:p.Phe1170=
ENST00000652107.1:c.3603_3615delinsTAATGCAGCAAGG (MSH6) ENSP00000498629.1:p.Phe1201=
ENST00000673637.1:c.3603_3615delinsTAATGCAGCAAGG (MSH6) ENSP00000501310.1:p.Phe1201=
ENST00000234420.9:c.3900_3912delinsTAATGCAGCAAGG (MSH6) ENSP00000234420.4:p.Phe1300=
ENST00000405808.5:c.169+1633_169+1645delinsCCTTGCTGCATTA (FBXO11) ENSP00000385127.1:n.169+1633_169+1645delinsCCTTGCTGCATTA
ENST00000434234.5:c.*124+1432_*124+1444delinsCCTTGCTGCATTA (FBXO11) ENSP00000402692.1:n.*124+1432_*124+1444delinsCCTTGCTGCATTA
ENST00000445503.5:c.*3247_*3259delinsTAATGCAGCAAGG (MSH6) ENSP00000405294.1:n.*3247_*3259delinsTAATGCAGCAAGG
ENST00000538136.1:c.2994_3006delinsTAATGCAGCAAGG (MSH6) ENSP00000438580.1:p.Phe998=
ENST00000540021.5:c.3510_3522delinsTAATGCAGCAAGG (MSH6) ENSP00000446475.1:p.Phe1170=
ENST00000614496.4:c.2994_3006delinsTAATGCAGCAAGG (MSH6) ENSP00000477844.1:p.Phe998=
ENST00000622629.4:c.801_813delinsTAATGCAGCAAGG (MSH6) ENSP00000482078.1:p.Phe267=
NM_000179.2:c.3900_3912delinsTAATGCAGCAAGG , LRG_219t1:c.3900_3912delinsTAATGCAGCAAGG (MSH6) NP_000170.1:p.Phe1300=
NM_001281492.1:c.3510_3522delinsTAATGCAGCAAGG (MSH6) NP_001268421.1:p.Phe1170=
NM_001281493.1:c.2994_3006delinsTAATGCAGCAAGG (MSH6) NP_001268422.1:p.Phe998=
NM_001281494.1:c.2994_3006delinsTAATGCAGCAAGG (MSH6) NP_001268423.1:p.Phe998=
XM_005264271.1:c.3603_3615delinsTAATGCAGCAAGG (MSH6) XP_005264328.1:p.Phe1201=
XM_011532798.1:c.3717_3729delinsTAATGCAGCAAGG (MSH6) XP_011531100.1:p.Phe1239=
XM_011532799.1:c.3603_3615delinsTAATGCAGCAAGG (MSH6) XP_011531101.1:p.Phe1201=
XM_011532800.1:c.3603_3615delinsTAATGCAGCAAGG (MSH6) XP_011531102.1:p.Phe1201=
XM_024452819.1:c.3993_4005delinsTAATGCAGCAAGG (MSH6) XP_024308587.1:p.Phe1331=
XM_024452820.1:c.3810_3822delinsTAATGCAGCAAGG (MSH6) XP_024308588.1:p.Phe1270=
XM_024452821.1:c.3696_3708delinsTAATGCAGCAAGG (MSH6) XP_024308589.1:p.Phe1232=
XM_024452822.1:c.3087_3099delinsTAATGCAGCAAGG (MSH6) XP_024308590.1:p.Phe1029=
NM_000179.3:c.3900_3912delinsTAATGCAGCAAGG (MSH6) MANE Select NP_000170.1:p.Phe1300=
NM_001281492.2:c.3510_3522delinsTAATGCAGCAAGG (MSH6) NP_001268421.1:p.Phe1170=
NM_001281493.2:c.2994_3006delinsTAATGCAGCAAGG (MSH6) NP_001268422.1:p.Phe998=
NM_001281494.2:c.2994_3006delinsTAATGCAGCAAGG (MSH6) NP_001268423.1:p.Phe998=