Canonical Allele Identifier: CA16617705

Linked Data

ClinVar Variation Id: 422205
dbSNP Id: rs1064795629

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806204del , CM000664.2:g.47806204del GRCh38
NC_000002.11:g.48033343del , CM000664.1:g.48033343del GRCh37
NC_000002.10:g.47886847del NCBI36
NG_007111.1:g.28058del , LRG_219:g.28058del
NG_008397.1:g.104473del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3350del (MSH6)
ENST00000420813.6:c.3350del (MSH6)
ENST00000455383.6:c.3350del (MSH6)
ENST00000700004.2:c.3263del (MSH6)
ENST00000699999.1:n.4321del (MSH6)
ENST00000700000.1:c.2081del (MSH6)
ENST00000700002.1:c.3653del (MSH6)
ENST00000700003.1:c.1102del (MSH6)
ENST00000700004.1:c.2420del (MSH6)
ENST00000700005.1:n.2498del (MSH6)
ENST00000700006.1:n.4805del (MSH6)
ENST00000700007.1:n.2242del (MSH6)
ENST00000700008.1:n.1816del (MSH6)
ENST00000700009.1:n.2311del (MSH6)
ENST00000700010.1:n.1056del (MSH6)
ENST00000700011.1:n.2941del (MSH6)
ENST00000682451.1:n.4545del (FBXO11)
ENST00000684712.1:n.4807del (FBXO11)
ENST00000234420.11:c.3647del (MSH6)
ENST00000540021.6:c.3257del (MSH6)
ENST00000652107.1:c.3350del (MSH6)
ENST00000673637.1:c.3350del (MSH6)
ENST00000234420.9:c.3647del (MSH6)
ENST00000405808.5:c.169+1992del (FBXO11) ENSP00000385127.1:n.169+1992del
ENST00000434234.5:c.*124+1791del (FBXO11) ENSP00000402692.1:n.*124+1791del
ENST00000445503.5:c.*2994del (MSH6)
ENST00000538136.1:c.2741del (MSH6)
ENST00000540021.5:c.3257del (MSH6)
ENST00000614496.4:c.2741del (MSH6)
ENST00000622629.4:c.551del (MSH6)
NM_000179.2:c.3647del , LRG_219t1:c.3647del (MSH6)
NM_001281492.1:c.3257del (MSH6)
NM_001281493.1:c.2741del (MSH6)
NM_001281494.1:c.2741del (MSH6)
XM_005264271.1:c.3350del (MSH6)
XM_011532798.1:c.3464del (MSH6)
XM_011532799.1:c.3350del (MSH6)
XM_011532800.1:c.3350del (MSH6)
XM_024452819.1:c.3647del (MSH6)
XM_024452820.1:c.3464del (MSH6)
XM_024452821.1:c.3350del (MSH6)
XM_024452822.1:c.2741del (MSH6)
NM_000179.3:c.3647del (MSH6)
NM_001281492.2:c.3257del (MSH6)
NM_001281493.2:c.2741del (MSH6)
NM_001281494.2:c.2741del (MSH6)