Canonical Allele Identifier: CA1672929639
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526926C= , CM000668.2:g.151526926C= GRCh38
NC_000006.11:g.151848061C= , CM000668.1:g.151848061C= GRCh37
NC_000006.10:g.151889754C= NCBI36
NG_021198.1:g.37887C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9392C= MANE Select ENSP00000239374.6:n.58-9392C=
ENST00000239374.7:c.58-9392C= ENSP00000239374.6:n.58-9392C=
NM_025059.3:c.58-9392C= NP_079335.2:n.58-9392C=
NM_025059.4:c.58-9392C= MANE Select NP_079335.2:n.58-9392C=
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