Canonical Allele Identifier: CA2496053187

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47805270_47805271delinsTC , CM000664.2:g.47805270_47805271delinsTC GRCh38
NC_000002.11:g.48032409_48032410delinsTC , CM000664.1:g.48032409_48032410delinsTC GRCh37
NC_000002.10:g.47885913_47885914delinsTC NCBI36
NG_007111.1:g.27124_27125delinsTC , LRG_219:g.27124_27125delinsTC
NG_008397.1:g.105405_105406delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3259+243_3259+244delinsTC (MSH6) ENSP00000406248.2:n.3259+243_3259+244delinsTC
ENST00000420813.6:c.3259+243_3259+244delinsTC (MSH6) ENSP00000390382.2:n.3259+243_3259+244delinsTC
ENST00000455383.6:c.3259+243_3259+244delinsTC (MSH6) ENSP00000397484.2:n.3259+243_3259+244delinsTC
ENST00000700004.2:c.3173-348_3173-347delinsTC (MSH6) ENSP00000514752.2:n.3173-348_3173-347delinsTC
ENST00000699999.1:n.3883_3884delinsTC (MSH6)
ENST00000700000.1:c.1990+243_1990+244delinsTC (MSH6) ENSP00000514749.1:n.1990+243_1990+244delinsTC
ENST00000700002.1:c.3562+243_3562+244delinsTC (MSH6) ENSP00000514750.1:n.3562+243_3562+244delinsTC
ENST00000700003.1:c.1011+243_1011+244delinsTC (MSH6) ENSP00000514751.1:n.1011+243_1011+244delinsTC
ENST00000700004.1:c.2330-348_2330-347delinsTC (MSH6) ENSP00000514752.1:n.2330-348_2330-347delinsTC
ENST00000700005.1:n.2407+243_2407+244delinsTC (MSH6)
ENST00000700006.1:n.3871_3872delinsTC (MSH6)
ENST00000700007.1:n.1804_1805delinsTC (MSH6)
ENST00000700008.1:n.1378_1379delinsTC (MSH6)
ENST00000700009.1:n.1377_1378delinsTC (MSH6)
ENST00000700010.1:n.965+243_965+244delinsTC (MSH6)
ENST00000700011.1:n.2503_2504delinsTC (MSH6)
ENST00000234420.11:c.3556+243_3556+244delinsTC (MSH6) MANE Select ENSP00000234420.5:n.3556+243_3556+244delinsTC
ENST00000540021.6:c.3166+243_3166+244delinsTC (MSH6) ENSP00000446475.1:n.3166+243_3166+244delinsTC
ENST00000652107.1:c.3259+243_3259+244delinsTC (MSH6) ENSP00000498629.1:n.3259+243_3259+244delinsTC
ENST00000673637.1:c.3259+243_3259+244delinsTC (MSH6) ENSP00000501310.1:n.3259+243_3259+244delinsTC
ENST00000234420.9:c.3556+243_3556+244delinsTC (MSH6) ENSP00000234420.4:n.3556+243_3556+244delinsTC
ENST00000405808.5:c.169+2924_169+2925delinsGA (FBXO11) ENSP00000385127.1:n.169+2924_169+2925delinsGA
ENST00000434234.5:c.*124+2723_*124+2724delinsGA (FBXO11) ENSP00000402692.1:n.*124+2723_*124+2724delinsGA
ENST00000445503.5:c.*2903+243_*2903+244delinsTC (MSH6) ENSP00000405294.1:n.*2903+243_*2903+244delinsTC
ENST00000538136.1:c.2650+243_2650+244delinsTC (MSH6) ENSP00000438580.1:n.2650+243_2650+244delinsTC
ENST00000540021.5:c.3166+243_3166+244delinsTC (MSH6) ENSP00000446475.1:n.3166+243_3166+244delinsTC
ENST00000614496.4:c.2650+243_2650+244delinsTC (MSH6) ENSP00000477844.1:n.2650+243_2650+244delinsTC
ENST00000622629.4:c.460+243_460+244delinsTC (MSH6) ENSP00000482078.1:n.460+243_460+244delinsTC
NM_000179.2:c.3556+243_3556+244delinsTC , LRG_219t1:c.3556+243_3556+244delinsTC (MSH6) NP_000170.1:n.3556+243_3556+244delinsTC
NM_001281492.1:c.3166+243_3166+244delinsTC (MSH6) NP_001268421.1:n.3166+243_3166+244delinsTC
NM_001281493.1:c.2650+243_2650+244delinsTC (MSH6) NP_001268422.1:n.2650+243_2650+244delinsTC
NM_001281494.1:c.2650+243_2650+244delinsTC (MSH6) NP_001268423.1:n.2650+243_2650+244delinsTC
XM_005264271.1:c.3259+243_3259+244delinsTC (MSH6) XP_005264328.1:n.3259+243_3259+244delinsTC
XM_011532798.1:c.3373+243_3373+244delinsTC (MSH6) XP_011531100.1:n.3373+243_3373+244delinsTC
XM_011532799.1:c.3259+243_3259+244delinsTC (MSH6) XP_011531101.1:n.3259+243_3259+244delinsTC
XM_011532800.1:c.3259+243_3259+244delinsTC (MSH6) XP_011531102.1:n.3259+243_3259+244delinsTC
XM_024452819.1:c.3556+243_3556+244delinsTC (MSH6) XP_024308587.1:n.3556+243_3556+244delinsTC
XM_024452820.1:c.3373+243_3373+244delinsTC (MSH6) XP_024308588.1:n.3373+243_3373+244delinsTC
XM_024452821.1:c.3259+243_3259+244delinsTC (MSH6) XP_024308589.1:n.3259+243_3259+244delinsTC
XM_024452822.1:c.2650+243_2650+244delinsTC (MSH6) XP_024308590.1:n.2650+243_2650+244delinsTC
NM_000179.3:c.3556+243_3556+244delinsTC (MSH6) MANE Select NP_000170.1:n.3556+243_3556+244delinsTC
NM_001281492.2:c.3166+243_3166+244delinsTC (MSH6) NP_001268421.1:n.3166+243_3166+244delinsTC
NM_001281493.2:c.2650+243_2650+244delinsTC (MSH6) NP_001268422.1:n.2650+243_2650+244delinsTC
NM_001281494.2:c.2650+243_2650+244delinsTC (MSH6) NP_001268423.1:n.2650+243_2650+244delinsTC