Canonical Allele Identifier: CA366067914

Gene: CCDC170

Linked Data

• MyVariant Identifiers: chr6:g.151936756C>T (hg19) ; chr6:g.151615621C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1889C>T MANE Select	ENSP00000239374.6:p.Thr630Ile
ENST00000239374.7:c.1889C>T	ENSP00000239374.6:p.Thr630Ile
NM_025059.3:c.1889C>T	NP_079335.2:p.Thr630Ile
XM_011536147.1:c.1907C>T	XP_011534449.1:p.Thr636Ile
XM_011536148.1:c.1706C>T	XP_011534450.1:p.Thr569Ile
XM_011536147.2:c.1907C>T	XP_011534449.1:p.Thr636Ile
XM_011536148.2:c.1706C>T	XP_011534450.1:p.Thr569Ile
XR_001743865.1:n.129+1100G>A
NM_025059.4:c.1889C>T MANE Select	NP_079335.2:p.Thr630Ile