Canonical Allele Identifier: CA1095909175
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs577450833
gnomAD v3: 6-151526519-CTTTTTT-C
gnomAD v4: 6-151526519-CTTTTTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526529_151526534del , CM000668.2:g.151526529_151526534del GRCh38
NC_000006.11:g.151847664_151847669del , CM000668.1:g.151847664_151847669del GRCh37
NC_000006.10:g.151889357_151889362del NCBI36
NG_021198.1:g.37490_37495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9789_58-9784del MANE Select ENSP00000239374.6:n.58-9789_58-9784del
ENST00000239374.7:c.58-9789_58-9784del ENSP00000239374.6:n.58-9789_58-9784del
NM_025059.3:c.58-9789_58-9784del NP_079335.2:n.58-9789_58-9784del
NM_025059.4:c.58-9789_58-9784del MANE Select NP_079335.2:n.58-9789_58-9784del
Search 100 bp 5'
Search 100 bp 3'