Canonical Allele Identifier: CA150139881

Gene: CCDC170

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151530204G>A , CM000668.2:g.151530204G>A	GRCh38
NC_000006.11:g.151851339G>A , CM000668.1:g.151851339G>A	GRCh37
NC_000006.10:g.151893032G>A	NCBI36
NG_021198.1:g.41165G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.58-6114G>A MANE Select	ENSP00000239374.6:n.58-6114G>A
ENST00000239374.7:c.58-6114G>A	ENSP00000239374.6:n.58-6114G>A
NM_025059.3:c.58-6114G>A	NP_079335.2:n.58-6114G>A
NM_025059.4:c.58-6114G>A MANE Select	NP_079335.2:n.58-6114G>A