Canonical Allele Identifier: CA820809541
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1269965110
gnomAD v3: 6-151580304-CT-C
gnomAD v4: 6-151580304-CT-C
MyVariant Identifiers: chr6:g.151901440del (hg19) chr6:g.151580305del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580306del , CM000668.2:g.151580306del GRCh38
NC_000006.11:g.151901441del , CM000668.1:g.151901441del GRCh37
NC_000006.10:g.151943134del NCBI36
NG_021198.1:g.91267del

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5583del MANE Select ENSP00000239374.6:n.1093-5583del
ENST00000239374.7:c.1093-5583del ENSP00000239374.6:n.1093-5583del
NM_025059.3:c.1093-5583del NP_079335.2:n.1093-5583del
XM_011536147.1:c.1111-5583del XP_011534449.1:n.1111-5583del
XM_011536148.1:c.1110+6815del XP_011534450.1:n.1110+6815del
XM_011536147.2:c.1111-5583del XP_011534449.1:n.1111-5583del
XM_011536148.2:c.1110+6815del XP_011534450.1:n.1110+6815del
NM_025059.4:c.1093-5583del MANE Select NP_079335.2:n.1093-5583del
Search 100 bp 5'
Search 100 bp 3'