Canonical Allele Identifier: CA452969730

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151615562-C-T
• MyVariant Identifiers: chr6:g.151936697C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615562C>T , CM000668.2:g.151615562C>T	GRCh38
NC_000006.11:g.151936697C>T , CM000668.1:g.151936697C>T	GRCh37
NC_000006.10:g.151978390C>T	NCBI36
NG_021198.1:g.126523C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1830C>T MANE Select	ENSP00000239374.6:p.Thr610=
ENST00000239374.7:c.1830C>T	ENSP00000239374.6:p.Thr610=
NM_025059.3:c.1830C>T	NP_079335.2:p.Thr610=
XM_011536147.1:c.1848C>T	XP_011534449.1:p.Thr616=
XM_011536148.1:c.1647C>T	XP_011534450.1:p.Thr549=
XM_011536147.2:c.1848C>T	XP_011534449.1:p.Thr616=
XM_011536148.2:c.1647C>T	XP_011534450.1:p.Thr549=
XR_001743865.1:n.129+1159G>A
NM_025059.4:c.1830C>T MANE Select	NP_079335.2:p.Thr610=