Canonical Allele Identifier: CA2514656969

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151526556G>C , CM000668.2:g.151526556G>C	GRCh38
NC_000006.11:g.151847691G>C , CM000668.1:g.151847691G>C	GRCh37
NC_000006.10:g.151889384G>C	NCBI36
NG_021198.1:g.37517G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.58-9762G>C MANE Select	ENSP00000239374.6:n.58-9762G>C
ENST00000239374.7:c.58-9762G>C	ENSP00000239374.6:n.58-9762G>C
NM_025059.3:c.58-9762G>C	NP_079335.2:n.58-9762G>C
NM_025059.4:c.58-9762G>C MANE Select	NP_079335.2:n.58-9762G>C