Canonical Allele Identifier: CA1095897025

Gene: CCDC170

Linked Data

• dbSNP Id: rs1777008672
• gnomAD v3: 6-151618632-C-T
• gnomAD v4: 6-151618632-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618632C>T , CM000668.2:g.151618632C>T	GRCh38
NC_000006.11:g.151939767C>T , CM000668.1:g.151939767C>T	GRCh37
NC_000006.10:g.151981460C>T	NCBI36
NG_021198.1:g.129593C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*485C>T MANE Select	ENSP00000239374.6:n.*485C>T
ENST00000239374.7:c.*485C>T	ENSP00000239374.6:n.*485C>T
NM_025059.3:c.*485C>T	NP_079335.2:n.*485C>T
XM_011536147.1:c.*485C>T	XP_011534449.1:n.*485C>T
XM_011536148.1:c.*485C>T	XP_011534450.1:n.*485C>T
XM_011536147.2:c.*485C>T	XP_011534449.1:n.*485C>T
XM_011536148.2:c.*485C>T	XP_011534450.1:n.*485C>T
NM_025059.4:c.*485C>T MANE Select	NP_079335.2:n.*485C>T