Canonical Allele Identifier: CA16617702

Linked Data

ClinVar Variation Id: 418872
dbSNP Id: rs1064793489

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47805028del , CM000664.2:g.47805028del GRCh38
NC_000002.11:g.48032167del , CM000664.1:g.48032167del GRCh37
NC_000002.10:g.47885671del NCBI36
NG_007111.1:g.26882del , LRG_219:g.26882del
NG_008397.1:g.105649del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3259+1del (MSH6)
ENST00000420813.6:c.3259+1del (MSH6)
ENST00000455383.6:c.3259+1del (MSH6)
ENST00000700004.2:c.3173-590del (MSH6) ENSP00000514752.2:n.3173-590del
ENST00000699999.1:n.3641del (MSH6)
ENST00000700000.1:c.1990+1del (MSH6)
ENST00000700002.1:c.3562+1del (MSH6)
ENST00000700003.1:c.1011+1del (MSH6)
ENST00000700004.1:c.2330-590del (MSH6) ENSP00000514752.1:n.2330-590del
ENST00000700005.1:n.2407+1del (MSH6)
ENST00000700006.1:n.3629del (MSH6)
ENST00000700007.1:n.1562del (MSH6)
ENST00000700008.1:n.1136del (MSH6)
ENST00000700009.1:n.1135del (MSH6)
ENST00000700010.1:n.965+1del (MSH6)
ENST00000700011.1:n.2261del (MSH6)
ENST00000234420.11:c.3556+1del (MSH6)
ENST00000540021.6:c.3166+1del (MSH6)
ENST00000652107.1:c.3259+1del (MSH6)
ENST00000673637.1:c.3259+1del (MSH6)
ENST00000234420.9:c.3556+1del (MSH6)
ENST00000405808.5:c.169+3168del (FBXO11) ENSP00000385127.1:n.169+3168del
ENST00000434234.5:c.*124+2967del (FBXO11) ENSP00000402692.1:n.*124+2967del
ENST00000445503.5:c.*2903+1del (MSH6)
ENST00000538136.1:c.2650+1del (MSH6)
ENST00000540021.5:c.3166+1del (MSH6)
ENST00000614496.4:c.2650+1del (MSH6)
ENST00000622629.4:c.460+1del (MSH6)
NM_000179.2:c.3556+1del , LRG_219t1:c.3556+1del (MSH6)
NM_001281492.1:c.3166+1del (MSH6)
NM_001281493.1:c.2650+1del (MSH6)
NM_001281494.1:c.2650+1del (MSH6)
XM_005264271.1:c.3259+1del (MSH6)
XM_011532798.1:c.3373+1del (MSH6)
XM_011532799.1:c.3259+1del (MSH6)
XM_011532800.1:c.3259+1del (MSH6)
XM_024452819.1:c.3556+1del (MSH6)
XM_024452820.1:c.3373+1del (MSH6)
XM_024452821.1:c.3259+1del (MSH6)
XM_024452822.1:c.2650+1del (MSH6)
NM_000179.3:c.3556+1del (MSH6)
NM_001281492.2:c.3166+1del (MSH6)
NM_001281493.2:c.2650+1del (MSH6)
NM_001281494.2:c.2650+1del (MSH6)