Canonical Allele Identifier: CA150160118
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs772179278
MyVariant Identifiers: chr6:g.151901352del (hg19) chr6:g.151580217del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580217del , CM000668.2:g.151580217del GRCh38
NC_000006.11:g.151901352del , CM000668.1:g.151901352del GRCh37
NC_000006.10:g.151943045del NCBI36
NG_021198.1:g.91178del

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5672del MANE Select ENSP00000239374.6:n.1093-5672del
ENST00000239374.7:c.1093-5672del ENSP00000239374.6:n.1093-5672del
NM_025059.3:c.1093-5672del NP_079335.2:n.1093-5672del
XM_011536147.1:c.1111-5672del XP_011534449.1:n.1111-5672del
XM_011536148.1:c.1110+6726del XP_011534450.1:n.1110+6726del
XM_011536147.2:c.1111-5672del XP_011534449.1:n.1111-5672del
XM_011536148.2:c.1110+6726del XP_011534450.1:n.1110+6726del
NM_025059.4:c.1093-5672del MANE Select NP_079335.2:n.1093-5672del
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