Canonical Allele Identifier: CA2680801694

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151618761-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618761A>G , CM000668.2:g.151618761A>G	GRCh38
NC_000006.11:g.151939896A>G , CM000668.1:g.151939896A>G	GRCh37
NC_000006.10:g.151981589A>G	NCBI36
NG_021198.1:g.129722A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*614A>G MANE Select	ENSP00000239374.6:n.*614A>G
ENST00000239374.7:c.*614A>G	ENSP00000239374.6:n.*614A>G
NM_025059.3:c.*614A>G	NP_079335.2:n.*614A>G
XM_011536147.1:c.*614A>G	XP_011534449.1:n.*614A>G
XM_011536148.1:c.*614A>G	XP_011534450.1:n.*614A>G
XM_011536147.2:c.*614A>G	XP_011534449.1:n.*614A>G
XM_011536148.2:c.*614A>G	XP_011534450.1:n.*614A>G
NM_025059.4:c.*614A>G MANE Select	NP_079335.2:n.*614A>G