Canonical Allele Identifier: CA150154138

Gene: CCDC170

Linked Data

• dbSNP Id: rs79928996
• MyVariant Identifiers: chr6:g.151933126G>C (hg19) ; chr6:g.151611991G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151611991G>C , CM000668.2:g.151611991G>C	GRCh38
NC_000006.11:g.151933126G>C , CM000668.1:g.151933126G>C	GRCh37
NC_000006.10:g.151974819G>C	NCBI36
NG_021198.1:g.122952G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1711-3452G>C MANE Select	ENSP00000239374.6:n.1711-3452G>C
ENST00000239374.7:c.1711-3452G>C	ENSP00000239374.6:n.1711-3452G>C
ENST00000537358.1:n.497-3452G>C
NM_025059.3:c.1711-3452G>C	NP_079335.2:n.1711-3452G>C
XM_011536147.1:c.1729-3452G>C	XP_011534449.1:n.1729-3452G>C
XM_011536148.1:c.1528-3452G>C	XP_011534450.1:n.1528-3452G>C
XM_011536147.2:c.1729-3452G>C	XP_011534449.1:n.1729-3452G>C
XM_011536148.2:c.1528-3452G>C	XP_011534450.1:n.1528-3452G>C
XR_001743865.1:n.130-719C>G
NM_025059.4:c.1711-3452G>C MANE Select	NP_079335.2:n.1711-3452G>C