Canonical Allele Identifier: CA2496054437

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806710_47806712delinsTAA , CM000664.2:g.47806710_47806712delinsTAA GRCh38
NC_000002.11:g.48033849_48033851delinsTAA , CM000664.1:g.48033849_48033851delinsTAA GRCh37
NC_000002.10:g.47887353_47887355delinsTAA NCBI36
NG_007111.1:g.28564_28566delinsTAA , LRG_219:g.28564_28566delinsTAA
NG_008397.1:g.103964_103966delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3704+59_3704+61delinsTAA (MSH6) ENSP00000406248.2:n.3704+59_3704+61delinsTAA
ENST00000420813.6:c.3704+59_3704+61delinsTAA (MSH6) ENSP00000390382.2:n.3704+59_3704+61delinsTAA
ENST00000455383.6:c.3704+59_3704+61delinsTAA (MSH6) ENSP00000397484.2:n.3704+59_3704+61delinsTAA
ENST00000700004.2:c.3617+59_3617+61delinsTAA (MSH6) ENSP00000514752.2:n.3617+59_3617+61delinsTAA
ENST00000699999.1:n.4675+59_4675+61delinsTAA (MSH6)
ENST00000700000.1:c.2435+59_2435+61delinsTAA (MSH6) ENSP00000514749.1:n.2435+59_2435+61delinsTAA
ENST00000700002.1:c.4007+59_4007+61delinsTAA (MSH6) ENSP00000514750.1:n.4007+59_4007+61delinsTAA
ENST00000700003.1:c.1456+59_1456+61delinsTAA (MSH6) ENSP00000514751.1:n.1456+59_1456+61delinsTAA
ENST00000700004.1:c.2774+59_2774+61delinsTAA (MSH6) ENSP00000514752.1:n.2774+59_2774+61delinsTAA
ENST00000700005.1:n.2911_2913delinsTAA (MSH6)
ENST00000700006.1:n.5218_5220delinsTAA (MSH6)
ENST00000700007.1:n.2596+59_2596+61delinsTAA (MSH6)
ENST00000700008.1:n.2263+59_2263+61delinsTAA (MSH6)
ENST00000700009.1:n.2665+59_2665+61delinsTAA (MSH6)
ENST00000700010.1:n.1410+59_1410+61delinsTAA (MSH6)
ENST00000700011.1:n.3295+59_3295+61delinsTAA (MSH6)
ENST00000682451.1:n.4036_4038delinsTTA (FBXO11)
ENST00000684712.1:n.4298_4300delinsTTA (FBXO11)
ENST00000234420.11:c.4001+59_4001+61delinsTAA (MSH6) MANE Select ENSP00000234420.5:n.4001+59_4001+61delinsTAA
ENST00000540021.6:c.3611+59_3611+61delinsTAA (MSH6) ENSP00000446475.1:n.3611+59_3611+61delinsTAA
ENST00000652107.1:c.3704+59_3704+61delinsTAA (MSH6) ENSP00000498629.1:n.3704+59_3704+61delinsTAA
ENST00000673637.1:c.3704+59_3704+61delinsTAA (MSH6) ENSP00000501310.1:n.3704+59_3704+61delinsTAA
ENST00000234420.9:c.4001+59_4001+61delinsTAA (MSH6) ENSP00000234420.4:n.4001+59_4001+61delinsTAA
ENST00000405808.5:c.169+1483_169+1485delinsTTA (FBXO11) ENSP00000385127.1:n.169+1483_169+1485delinsTTA
ENST00000434234.5:c.*124+1282_*124+1284delinsTTA (FBXO11) ENSP00000402692.1:n.*124+1282_*124+1284delinsTTA
ENST00000445503.5:c.*3348+59_*3348+61delinsTAA (MSH6) ENSP00000405294.1:n.*3348+59_*3348+61delinsTAA
ENST00000538136.1:c.3095+59_3095+61delinsTAA (MSH6) ENSP00000438580.1:n.3095+59_3095+61delinsTAA
ENST00000540021.5:c.3611+59_3611+61delinsTAA (MSH6) ENSP00000446475.1:n.3611+59_3611+61delinsTAA
ENST00000614496.4:c.3095+59_3095+61delinsTAA (MSH6) ENSP00000477844.1:n.3095+59_3095+61delinsTAA
ENST00000622629.4:c.902+59_902+61delinsTAA (MSH6) ENSP00000482078.1:n.902+59_902+61delinsTAA
NM_000179.2:c.4001+59_4001+61delinsTAA , LRG_219t1:c.4001+59_4001+61delinsTAA (MSH6) NP_000170.1:n.4001+59_4001+61delinsTAA
NM_001281492.1:c.3611+59_3611+61delinsTAA (MSH6) NP_001268421.1:n.3611+59_3611+61delinsTAA
NM_001281493.1:c.3095+59_3095+61delinsTAA (MSH6) NP_001268422.1:n.3095+59_3095+61delinsTAA
NM_001281494.1:c.3095+59_3095+61delinsTAA (MSH6) NP_001268423.1:n.3095+59_3095+61delinsTAA
XM_005264271.1:c.3704+59_3704+61delinsTAA (MSH6) XP_005264328.1:n.3704+59_3704+61delinsTAA
XM_011532798.1:c.3818+59_3818+61delinsTAA (MSH6) XP_011531100.1:n.3818+59_3818+61delinsTAA
XM_011532799.1:c.3704+59_3704+61delinsTAA (MSH6) XP_011531101.1:n.3704+59_3704+61delinsTAA
XM_011532800.1:c.3704+59_3704+61delinsTAA (MSH6) XP_011531102.1:n.3704+59_3704+61delinsTAA
XM_024452819.1:c.4094+59_4094+61delinsTAA (MSH6) XP_024308587.1:n.4094+59_4094+61delinsTAA
XM_024452820.1:c.3911+59_3911+61delinsTAA (MSH6) XP_024308588.1:n.3911+59_3911+61delinsTAA
XM_024452821.1:c.3797+59_3797+61delinsTAA (MSH6) XP_024308589.1:n.3797+59_3797+61delinsTAA
XM_024452822.1:c.3188+59_3188+61delinsTAA (MSH6) XP_024308590.1:n.3188+59_3188+61delinsTAA
NM_000179.3:c.4001+59_4001+61delinsTAA (MSH6) MANE Select NP_000170.1:n.4001+59_4001+61delinsTAA
NM_001281492.2:c.3611+59_3611+61delinsTAA (MSH6) NP_001268421.1:n.3611+59_3611+61delinsTAA
NM_001281493.2:c.3095+59_3095+61delinsTAA (MSH6) NP_001268422.1:n.3095+59_3095+61delinsTAA
NM_001281494.2:c.3095+59_3095+61delinsTAA (MSH6) NP_001268423.1:n.3095+59_3095+61delinsTAA