Canonical Allele Identifier: CA1672929557
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526735_151526736delinsAT , CM000668.2:g.151526735_151526736delinsAT GRCh38
NC_000006.11:g.151847870_151847871delinsAT , CM000668.1:g.151847870_151847871delinsAT GRCh37
NC_000006.10:g.151889563_151889564delinsAT NCBI36
NG_021198.1:g.37696_37697delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9583_58-9582delinsAT MANE Select ENSP00000239374.6:n.58-9583_58-9582delins...
ENST00000239374.7:c.58-9583_58-9582delinsAT ENSP00000239374.6:n.58-9583_58-9582delins...
NM_025059.3:c.58-9583_58-9582delinsAT NP_079335.2:n.58-9583_58-9582delinsAT
NM_025059.4:c.58-9583_58-9582delinsAT MANE Select NP_079335.2:n.58-9583_58-9582delinsAT