Canonical Allele Identifier: CA2680801460

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151618576-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618576G>T , CM000668.2:g.151618576G>T	GRCh38
NC_000006.11:g.151939711G>T , CM000668.1:g.151939711G>T	GRCh37
NC_000006.10:g.151981404G>T	NCBI36
NG_021198.1:g.129537G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*429G>T MANE Select	ENSP00000239374.6:n.*429G>T
ENST00000239374.7:c.*429G>T	ENSP00000239374.6:n.*429G>T
NM_025059.3:c.*429G>T	NP_079335.2:n.*429G>T
XM_011536147.1:c.*429G>T	XP_011534449.1:n.*429G>T
XM_011536148.1:c.*429G>T	XP_011534450.1:n.*429G>T
XM_011536147.2:c.*429G>T	XP_011534449.1:n.*429G>T
XM_011536148.2:c.*429G>T	XP_011534450.1:n.*429G>T
NM_025059.4:c.*429G>T MANE Select	NP_079335.2:n.*429G>T