Canonical Allele Identifier: CA1095909345
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526548G>C , CM000668.2:g.151526548G>C GRCh38
NC_000006.11:g.151847683G>C , CM000668.1:g.151847683G>C GRCh37
NC_000006.10:g.151889376G>C NCBI36
NG_021198.1:g.37509G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9770G>C MANE Select ENSP00000239374.6:n.58-9770G>C
ENST00000239374.7:c.58-9770G>C ENSP00000239374.6:n.58-9770G>C
NM_025059.3:c.58-9770G>C NP_079335.2:n.58-9770G>C
NM_025059.4:c.58-9770G>C MANE Select NP_079335.2:n.58-9770G>C