Canonical Allele Identifier: CA1139656956

Linked Data

ClinVar Variation Id: 850678
ClinVar RCV Id: RCV001054898

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47803431_47807699del , CM000664.2:g.47803431_47807699del GRCh38
NC_000002.11:g.48030570_48034838del , CM000664.1:g.48030570_48034838del GRCh37
NC_000002.10:g.47884074_47888342del NCBI36
NG_007111.1:g.25285_29553del , LRG_219:g.25285_29553del

Transcript Alleles

HGVS Amino-acid change
ENST00000652107.1:c.2887_*839del (MSH6)
ENST00000234420.9:c.3184_*839del (MSH6)
ENST00000405808.5:c.169+498_169+4766del (FBXO11) ENSP00000385127.1:n.169+498_169+4766del
ENST00000434234.5:c.*124+297_*124+4565del (FBXO11) ENSP00000402692.1:n.*124+297_*124+4565del...