Canonical Allele Identifier: CA366067361
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151936686G>C (hg19) chr6:g.151615551G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615551G>C , CM000668.2:g.151615551G>C GRCh38
NC_000006.11:g.151936686G>C , CM000668.1:g.151936686G>C GRCh37
NC_000006.10:g.151978379G>C NCBI36
NG_021198.1:g.126512G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1819G>C MANE Select ENSP00000239374.6:p.Glu607Gln
ENST00000239374.7:c.1819G>C ENSP00000239374.6:p.Glu607Gln
NM_025059.3:c.1819G>C NP_079335.2:p.Glu607Gln
XM_011536147.1:c.1837G>C XP_011534449.1:p.Glu613Gln
XM_011536148.1:c.1636G>C XP_011534450.1:p.Glu546Gln
XM_011536147.2:c.1837G>C XP_011534449.1:p.Glu613Gln
XM_011536148.2:c.1636G>C XP_011534450.1:p.Glu546Gln
XR_001743865.1:n.129+1170C>G
NM_025059.4:c.1819G>C MANE Select NP_079335.2:p.Glu607Gln
Search 100 bp 5'
Search 100 bp 3'