Canonical Allele Identifier: CA150138024
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1044497683
gnomAD v3: 6-151526895-ATT-A
gnomAD v4: 6-151526895-ATT-A
MyVariant Identifiers: chr6:g.151848031_151848032del (hg19) chr6:g.151526896_151526897del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526902_151526903del , CM000668.2:g.151526902_151526903del GRCh38
NC_000006.11:g.151848037_151848038del , CM000668.1:g.151848037_151848038del GRCh37
NC_000006.10:g.151889730_151889731del NCBI36
NG_021198.1:g.37863_37864del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9416_58-9415del MANE Select ENSP00000239374.6:n.58-9416_58-9415del
ENST00000239374.7:c.58-9416_58-9415del ENSP00000239374.6:n.58-9416_58-9415del
NM_025059.3:c.58-9416_58-9415del NP_079335.2:n.58-9416_58-9415del
NM_025059.4:c.58-9416_58-9415del MANE Select NP_079335.2:n.58-9416_58-9415del
Search 100 bp 5'
Search 100 bp 3'