Canonical Allele Identifier: CA452969744
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151936724A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615589A>G , CM000668.2:g.151615589A>G GRCh38
NC_000006.11:g.151936724A>G , CM000668.1:g.151936724A>G GRCh37
NC_000006.10:g.151978417A>G NCBI36
NG_021198.1:g.126550A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1857A>G MANE Select ENSP00000239374.6:p.Lys619=
ENST00000239374.7:c.1857A>G ENSP00000239374.6:p.Lys619=
NM_025059.3:c.1857A>G NP_079335.2:p.Lys619=
XM_011536147.1:c.1875A>G XP_011534449.1:p.Lys625=
XM_011536148.1:c.1674A>G XP_011534450.1:p.Lys558=
XM_011536147.2:c.1875A>G XP_011534449.1:p.Lys625=
XM_011536148.2:c.1674A>G XP_011534450.1:p.Lys558=
XR_001743865.1:n.129+1132T>C
NM_025059.4:c.1857A>G MANE Select NP_079335.2:p.Lys619=
Search 100 bp 5'
Search 100 bp 3'