Canonical Allele Identifier: CA2658967380

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806063_47806081dup , CM000664.2:g.47806063_47806081dup GRCh38
NC_000002.11:g.48033202_48033220dup , CM000664.1:g.48033202_48033220dup GRCh37
NC_000002.10:g.47886706_47886724dup NCBI36
NG_007111.1:g.27917_27935dup , LRG_219:g.27917_27935dup
NG_008397.1:g.104595_104613dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3350-141_3350-123dup (MSH6) ENSP00000406248.2:n.3350-141_3350-123dup
ENST00000420813.6:c.3350-141_3350-123dup (MSH6) ENSP00000390382.2:n.3350-141_3350-123dup
ENST00000455383.6:c.3350-141_3350-123dup (MSH6) ENSP00000397484.2:n.3350-141_3350-123dup
ENST00000700004.2:c.3263-141_3263-123dup (MSH6) ENSP00000514752.2:n.3263-141_3263-123dup
ENST00000699999.1:n.4321-141_4321-123dup (MSH6)
ENST00000700000.1:c.2081-141_2081-123dup (MSH6) ENSP00000514749.1:n.2081-141_2081-123dup
ENST00000700002.1:c.3653-141_3653-123dup (MSH6) ENSP00000514750.1:n.3653-141_3653-123dup
ENST00000700003.1:c.1102-141_1102-123dup (MSH6) ENSP00000514751.1:n.1102-141_1102-123dup
ENST00000700004.1:c.2420-141_2420-123dup (MSH6) ENSP00000514752.1:n.2420-141_2420-123dup
ENST00000700005.1:n.2498-141_2498-123dup (MSH6)
ENST00000700006.1:n.4664_4682dup (MSH6)
ENST00000700007.1:n.2242-141_2242-123dup (MSH6)
ENST00000700008.1:n.1816-141_1816-123dup (MSH6)
ENST00000700009.1:n.2170_2188dup (MSH6)
ENST00000700010.1:n.1056-141_1056-123dup (MSH6)
ENST00000700011.1:n.2941-141_2941-123dup (MSH6)
ENST00000682451.1:n.4667_4685dup (FBXO11)
ENST00000684712.1:n.4929_4947dup (FBXO11)
ENST00000234420.11:c.3647-141_3647-123dup (MSH6) MANE Select ENSP00000234420.5:n.3647-141_3647-123dup
ENST00000540021.6:c.3257-141_3257-123dup (MSH6) ENSP00000446475.1:n.3257-141_3257-123dup
ENST00000652107.1:c.3350-141_3350-123dup (MSH6) ENSP00000498629.1:n.3350-141_3350-123dup
ENST00000673637.1:c.3350-141_3350-123dup (MSH6) ENSP00000501310.1:n.3350-141_3350-123dup
ENST00000234420.9:c.3647-141_3647-123dup (MSH6) ENSP00000234420.4:n.3647-141_3647-123dup
ENST00000405808.5:c.169+2114_169+2132dup (FBXO11) ENSP00000385127.1:n.169+2114_169+2132dup
ENST00000434234.5:c.*124+1913_*124+1931dup (FBXO11) ENSP00000402692.1:n.*124+1913_*124+1931dup
ENST00000445503.5:c.*2994-141_*2994-123dup (MSH6) ENSP00000405294.1:n.*2994-141_*2994-123dup
ENST00000538136.1:c.2741-141_2741-123dup (MSH6) ENSP00000438580.1:n.2741-141_2741-123dup
ENST00000540021.5:c.3257-141_3257-123dup (MSH6) ENSP00000446475.1:n.3257-141_3257-123dup
ENST00000614496.4:c.2741-141_2741-123dup (MSH6) ENSP00000477844.1:n.2741-141_2741-123dup
ENST00000622629.4:c.551-141_551-123dup (MSH6) ENSP00000482078.1:n.551-141_551-123dup
NM_000179.2:c.3647-141_3647-123dup , LRG_219t1:c.3647-141_3647-123dup (MSH6) NP_000170.1:n.3647-141_3647-123dup
NM_001281492.1:c.3257-141_3257-123dup (MSH6) NP_001268421.1:n.3257-141_3257-123dup
NM_001281493.1:c.2741-141_2741-123dup (MSH6) NP_001268422.1:n.2741-141_2741-123dup
NM_001281494.1:c.2741-141_2741-123dup (MSH6) NP_001268423.1:n.2741-141_2741-123dup
XM_005264271.1:c.3350-141_3350-123dup (MSH6) XP_005264328.1:n.3350-141_3350-123dup
XM_011532798.1:c.3464-141_3464-123dup (MSH6) XP_011531100.1:n.3464-141_3464-123dup
XM_011532799.1:c.3350-141_3350-123dup (MSH6) XP_011531101.1:n.3350-141_3350-123dup
XM_011532800.1:c.3350-141_3350-123dup (MSH6) XP_011531102.1:n.3350-141_3350-123dup
XM_024452819.1:c.3647-141_3647-123dup (MSH6) XP_024308587.1:n.3647-141_3647-123dup
XM_024452820.1:c.3464-141_3464-123dup (MSH6) XP_024308588.1:n.3464-141_3464-123dup
XM_024452821.1:c.3350-141_3350-123dup (MSH6) XP_024308589.1:n.3350-141_3350-123dup
XM_024452822.1:c.2741-141_2741-123dup (MSH6) XP_024308590.1:n.2741-141_2741-123dup
NM_000179.3:c.3647-141_3647-123dup (MSH6) MANE Select NP_000170.1:n.3647-141_3647-123dup
NM_001281492.2:c.3257-141_3257-123dup (MSH6) NP_001268421.1:n.3257-141_3257-123dup
NM_001281493.2:c.2741-141_2741-123dup (MSH6) NP_001268422.1:n.2741-141_2741-123dup
NM_001281494.2:c.2741-141_2741-123dup (MSH6) NP_001268423.1:n.2741-141_2741-123dup