Canonical Allele Identifier: CA2680801235

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151618337-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618337C>T , CM000668.2:g.151618337C>T	GRCh38
NC_000006.11:g.151939472C>T , CM000668.1:g.151939472C>T	GRCh37
NC_000006.10:g.151981165C>T	NCBI36
NG_021198.1:g.129298C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*190C>T MANE Select	ENSP00000239374.6:n.*190C>T
ENST00000239374.7:c.*190C>T	ENSP00000239374.6:n.*190C>T
NM_025059.3:c.*190C>T	NP_079335.2:n.*190C>T
XM_011536147.1:c.*190C>T	XP_011534449.1:n.*190C>T
XM_011536148.1:c.*190C>T	XP_011534450.1:n.*190C>T
XM_011536147.2:c.*190C>T	XP_011534449.1:n.*190C>T
XM_011536148.2:c.*190C>T	XP_011534450.1:n.*190C>T
NM_025059.4:c.*190C>T MANE Select	NP_079335.2:n.*190C>T