Canonical Allele Identifier: CA1672965902

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618151_151618153delinsCTG , CM000668.2:g.151618151_151618153delinsCTG	GRCh38
NC_000006.11:g.151939286_151939288delinsCTG , CM000668.1:g.151939286_151939288delinsCTG	GRCh37
NC_000006.10:g.151980979_151980981delinsCTG	NCBI36
NG_021198.1:g.129112_129114delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*4_*6delinsCTG MANE Select	ENSP00000239374.6:n.*4_*6delinsCTG
ENST00000239374.7:c.*4_*6delinsCTG	ENSP00000239374.6:n.*4_*6delinsCTG
NM_025059.3:c.*4_*6delinsCTG	NP_079335.2:n.*4_*6delinsCTG
XM_011536147.1:c.*4_*6delinsCTG	XP_011534449.1:n.*4_*6delinsCTG
XM_011536148.1:c.*4_*6delinsCTG	XP_011534450.1:n.*4_*6delinsCTG
XM_011536147.2:c.*4_*6delinsCTG	XP_011534449.1:n.*4_*6delinsCTG
XM_011536148.2:c.*4_*6delinsCTG	XP_011534450.1:n.*4_*6delinsCTG
NM_025059.4:c.*4_*6delinsCTG MANE Select	NP_079335.2:n.*4_*6delinsCTG