Canonical Allele Identifier: CA1672929530
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526664G= , CM000668.2:g.151526664G= GRCh38
NC_000006.11:g.151847799G= , CM000668.1:g.151847799G= GRCh37
NC_000006.10:g.151889492G= NCBI36
NG_021198.1:g.37625G=

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9654G= MANE Select ENSP00000239374.6:n.58-9654G=
ENST00000239374.7:c.58-9654G= ENSP00000239374.6:n.58-9654G=
NM_025059.3:c.58-9654G= NP_079335.2:n.58-9654G=
NM_025059.4:c.58-9654G= MANE Select NP_079335.2:n.58-9654G=
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