Canonical Allele Identifier: CA452969701
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151936679C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615544C>A , CM000668.2:g.151615544C>A GRCh38
NC_000006.11:g.151936679C>A , CM000668.1:g.151936679C>A GRCh37
NC_000006.10:g.151978372C>A NCBI36
NG_021198.1:g.126505C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1812C>A MANE Select ENSP00000239374.6:p.Val604=
ENST00000239374.7:c.1812C>A ENSP00000239374.6:p.Val604=
NM_025059.3:c.1812C>A NP_079335.2:p.Val604=
XM_011536147.1:c.1830C>A XP_011534449.1:p.Val610=
XM_011536148.1:c.1629C>A XP_011534450.1:p.Val543=
XM_011536147.2:c.1830C>A XP_011534449.1:p.Val610=
XM_011536148.2:c.1629C>A XP_011534450.1:p.Val543=
XR_001743865.1:n.129+1177G>T
NM_025059.4:c.1812C>A MANE Select NP_079335.2:p.Val604=
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