Canonical Allele Identifier: CA366066587
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151936577G>A (hg19) chr6:g.151615442G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615442G>A , CM000668.2:g.151615442G>A GRCh38
NC_000006.11:g.151936577G>A , CM000668.1:g.151936577G>A GRCh37
NC_000006.10:g.151978270G>A NCBI36
NG_021198.1:g.126403G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1711-1G>A MANE Select ENSP00000239374.6:n.1711-1G>A
ENST00000239374.7:c.1711-1G>A ENSP00000239374.6:n.1711-1G>A
ENST00000537358.1:n.497-1G>A
NM_025059.3:c.1711-1G>A NP_079335.2:n.1711-1G>A
XM_011536147.1:c.1729-1G>A XP_011534449.1:n.1729-1G>A
XM_011536148.1:c.1528-1G>A XP_011534450.1:n.1528-1G>A
XM_011536147.2:c.1729-1G>A XP_011534449.1:n.1729-1G>A
XM_011536148.2:c.1528-1G>A XP_011534450.1:n.1528-1G>A
XR_001743865.1:n.129+1279C>T
NM_025059.4:c.1711-1G>A MANE Select NP_079335.2:n.1711-1G>A
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