Canonical Allele Identifier: CA366067913
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151936756C>A (hg19) chr6:g.151615621C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615621C>A , CM000668.2:g.151615621C>A GRCh38
NC_000006.11:g.151936756C>A , CM000668.1:g.151936756C>A GRCh37
NC_000006.10:g.151978449C>A NCBI36
NG_021198.1:g.126582C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1889C>A MANE Select ENSP00000239374.6:p.Thr630Asn
ENST00000239374.7:c.1889C>A ENSP00000239374.6:p.Thr630Asn
NM_025059.3:c.1889C>A NP_079335.2:p.Thr630Asn
XM_011536147.1:c.1907C>A XP_011534449.1:p.Thr636Asn
XM_011536148.1:c.1706C>A XP_011534450.1:p.Thr569Asn
XM_011536147.2:c.1907C>A XP_011534449.1:p.Thr636Asn
XM_011536148.2:c.1706C>A XP_011534450.1:p.Thr569Asn
XR_001743865.1:n.129+1100G>T
NM_025059.4:c.1889C>A MANE Select NP_079335.2:p.Thr630Asn
Search 100 bp 5'
Search 100 bp 3'