Canonical Allele Identifier: CA150156359
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs68158459
gnomAD v2: 6-151939760-TCTC-T
gnomAD v3: 6-151618625-TCTC-T
gnomAD v4: 6-151618625-TCTC-T
MyVariant Identifiers: chr6:g.151939761_151939763del (hg19) chr6:g.151618626_151618628del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618628_151618630del , CM000668.2:g.151618628_151618630del GRCh38
NC_000006.11:g.151939763_151939765del , CM000668.1:g.151939763_151939765del GRCh37
NC_000006.10:g.151981456_151981458del NCBI36
NG_021198.1:g.129589_129591del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*481_*483del MANE Select ENSP00000239374.6:n.*481_*483del
ENST00000239374.7:c.*481_*483del ENSP00000239374.6:n.*481_*483del
NM_025059.3:c.*481_*483del NP_079335.2:n.*481_*483del
XM_011536147.1:c.*481_*483del XP_011534449.1:n.*481_*483del
XM_011536148.1:c.*481_*483del XP_011534450.1:n.*481_*483del
XM_011536147.2:c.*481_*483del XP_011534449.1:n.*481_*483del
XM_011536148.2:c.*481_*483del XP_011534450.1:n.*481_*483del
NM_025059.4:c.*481_*483del MANE Select NP_079335.2:n.*481_*483del
Search 100 bp 5'
Search 100 bp 3'