Canonical Allele Identifier: CA1672929534
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526670_151526671delinsGC , CM000668.2:g.151526670_151526671delinsGC GRCh38
NC_000006.11:g.151847805_151847806delinsGC , CM000668.1:g.151847805_151847806delinsGC GRCh37
NC_000006.10:g.151889498_151889499delinsGC NCBI36
NG_021198.1:g.37631_37632delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9648_58-9647delinsGC MANE Select ENSP00000239374.6:n.58-9648_58-9647delinsGC
ENST00000239374.7:c.58-9648_58-9647delinsGC ENSP00000239374.6:n.58-9648_58-9647delinsGC
NM_025059.3:c.58-9648_58-9647delinsGC NP_079335.2:n.58-9648_58-9647delinsGC
NM_025059.4:c.58-9648_58-9647delinsGC MANE Select NP_079335.2:n.58-9648_58-9647delinsGC