Canonical Allele Identifier: CA366067469

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151615569-C-A
• MyVariant Identifiers: chr6:g.151936704C>A (hg19) ; chr6:g.151615569C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615569C>A , CM000668.2:g.151615569C>A	GRCh38
NC_000006.11:g.151936704C>A , CM000668.1:g.151936704C>A	GRCh37
NC_000006.10:g.151978397C>A	NCBI36
NG_021198.1:g.126530C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1837C>A MANE Select	ENSP00000239374.6:p.His613Asn
ENST00000239374.7:c.1837C>A	ENSP00000239374.6:p.His613Asn
NM_025059.3:c.1837C>A	NP_079335.2:p.His613Asn
XM_011536147.1:c.1855C>A	XP_011534449.1:p.His619Asn
XM_011536148.1:c.1654C>A	XP_011534450.1:p.His552Asn
XM_011536147.2:c.1855C>A	XP_011534449.1:p.His619Asn
XM_011536148.2:c.1654C>A	XP_011534450.1:p.His552Asn
XR_001743865.1:n.129+1152G>T
NM_025059.4:c.1837C>A MANE Select	NP_079335.2:p.His613Asn