Canonical Allele Identifier: CA072562

Linked Data

dbSNP Id: rs587779303

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806695_47806699dup , CM000664.2:g.47806695_47806699dup GRCh38
NC_000002.11:g.48033834_48033838dup , CM000664.1:g.48033834_48033838dup GRCh37
NC_000002.10:g.47887338_47887342dup NCBI36
NG_007111.1:g.28549_28553dup , LRG_219:g.28549_28553dup
NG_008397.1:g.103977_103981dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3704+44_3704+48dup (MSH6) ENSP00000406248.2:n.3704+44_3704+48dup
ENST00000420813.6:c.3704+44_3704+48dup (MSH6) ENSP00000390382.2:n.3704+44_3704+48dup
ENST00000455383.6:c.3704+44_3704+48dup (MSH6) ENSP00000397484.2:n.3704+44_3704+48dup
ENST00000700004.2:c.3617+44_3617+48dup (MSH6) ENSP00000514752.2:n.3617+44_3617+48dup
ENST00000699999.1:n.4675+44_4675+48dup (MSH6)
ENST00000700000.1:c.2435+44_2435+48dup (MSH6) ENSP00000514749.1:n.2435+44_2435+48dup
ENST00000700002.1:c.4007+44_4007+48dup (MSH6) ENSP00000514750.1:n.4007+44_4007+48dup
ENST00000700003.1:c.1456+44_1456+48dup (MSH6) ENSP00000514751.1:n.1456+44_1456+48dup
ENST00000700004.1:c.2774+44_2774+48dup (MSH6) ENSP00000514752.1:n.2774+44_2774+48dup
ENST00000700005.1:n.2896_2900dup (MSH6)
ENST00000700006.1:n.5203_5207dup (MSH6)
ENST00000700007.1:n.2596+44_2596+48dup (MSH6)
ENST00000700008.1:n.2263+44_2263+48dup (MSH6)
ENST00000700009.1:n.2665+44_2665+48dup (MSH6)
ENST00000700010.1:n.1410+44_1410+48dup (MSH6)
ENST00000700011.1:n.3295+44_3295+48dup (MSH6)
ENST00000682451.1:n.4049_4053dup (FBXO11)
ENST00000684712.1:n.4311_4315dup (FBXO11)
ENST00000234420.11:c.4001+44_4001+48dup (MSH6) MANE Select ENSP00000234420.5:n.4001+44_4001+48dup
ENST00000540021.6:c.3611+44_3611+48dup (MSH6) ENSP00000446475.1:n.3611+44_3611+48dup
ENST00000652107.1:c.3704+44_3704+48dup (MSH6) ENSP00000498629.1:n.3704+44_3704+48dup
ENST00000673637.1:c.3704+44_3704+48dup (MSH6) ENSP00000501310.1:n.3704+44_3704+48dup
ENST00000234420.9:c.4001+44_4001+48dup (MSH6) ENSP00000234420.4:n.4001+44_4001+48dup
ENST00000405808.5:c.169+1496_169+1500dup (FBXO11) ENSP00000385127.1:n.169+1496_169+1500dup
ENST00000434234.5:c.*124+1295_*124+1299dup (FBXO11) ENSP00000402692.1:n.*124+1295_*124+1299dup
ENST00000445503.5:c.*3348+44_*3348+48dup (MSH6) ENSP00000405294.1:n.*3348+44_*3348+48dup
ENST00000538136.1:c.3095+44_3095+48dup (MSH6) ENSP00000438580.1:n.3095+44_3095+48dup
ENST00000540021.5:c.3611+44_3611+48dup (MSH6) ENSP00000446475.1:n.3611+44_3611+48dup
ENST00000614496.4:c.3095+44_3095+48dup (MSH6) ENSP00000477844.1:n.3095+44_3095+48dup
ENST00000622629.4:c.902+44_902+48dup (MSH6) ENSP00000482078.1:n.902+44_902+48dup
NM_000179.2:c.4001+44_4001+48dup , LRG_219t1:c.4001+44_4001+48dup (MSH6) NP_000170.1:n.4001+44_4001+48dup
NM_001281492.1:c.3611+44_3611+48dup (MSH6) NP_001268421.1:n.3611+44_3611+48dup
NM_001281493.1:c.3095+44_3095+48dup (MSH6) NP_001268422.1:n.3095+44_3095+48dup
NM_001281494.1:c.3095+44_3095+48dup (MSH6) NP_001268423.1:n.3095+44_3095+48dup
XM_005264271.1:c.3704+44_3704+48dup (MSH6) XP_005264328.1:n.3704+44_3704+48dup
XM_011532798.1:c.3818+44_3818+48dup (MSH6) XP_011531100.1:n.3818+44_3818+48dup
XM_011532799.1:c.3704+44_3704+48dup (MSH6) XP_011531101.1:n.3704+44_3704+48dup
XM_011532800.1:c.3704+44_3704+48dup (MSH6) XP_011531102.1:n.3704+44_3704+48dup
XM_024452819.1:c.4094+44_4094+48dup (MSH6) XP_024308587.1:n.4094+44_4094+48dup
XM_024452820.1:c.3911+44_3911+48dup (MSH6) XP_024308588.1:n.3911+44_3911+48dup
XM_024452821.1:c.3797+44_3797+48dup (MSH6) XP_024308589.1:n.3797+44_3797+48dup
XM_024452822.1:c.3188+44_3188+48dup (MSH6) XP_024308590.1:n.3188+44_3188+48dup
NM_000179.3:c.4001+44_4001+48dup (MSH6) MANE Select NP_000170.1:n.4001+44_4001+48dup
NM_001281492.2:c.3611+44_3611+48dup (MSH6) NP_001268421.1:n.3611+44_3611+48dup
NM_001281493.2:c.3095+44_3095+48dup (MSH6) NP_001268422.1:n.3095+44_3095+48dup
NM_001281494.2:c.3095+44_3095+48dup (MSH6) NP_001268423.1:n.3095+44_3095+48dup