Canonical Allele Identifier: CA150160104

Gene: CCDC170

Linked Data

• dbSNP Id: rs981573699
• MyVariant Identifiers: chr6:g.151901340T>G (hg19) ; chr6:g.151580205T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151580205T>G , CM000668.2:g.151580205T>G	GRCh38
NC_000006.11:g.151901340T>G , CM000668.1:g.151901340T>G	GRCh37
NC_000006.10:g.151943033T>G	NCBI36
NG_021198.1:g.91166T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1093-5684T>G MANE Select	ENSP00000239374.6:n.1093-5684T>G
ENST00000239374.7:c.1093-5684T>G	ENSP00000239374.6:n.1093-5684T>G
NM_025059.3:c.1093-5684T>G	NP_079335.2:n.1093-5684T>G
XM_011536147.1:c.1111-5684T>G	XP_011534449.1:n.1111-5684T>G
XM_011536148.1:c.1110+6714T>G	XP_011534450.1:n.1110+6714T>G
XM_011536147.2:c.1111-5684T>G	XP_011534449.1:n.1111-5684T>G
XM_011536148.2:c.1110+6714T>G	XP_011534450.1:n.1110+6714T>G
NM_025059.4:c.1093-5684T>G MANE Select	NP_079335.2:n.1093-5684T>G