Canonical Allele Identifier: CA366069872
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618140T>G , CM000668.2:g.151618140T>G GRCh38
NC_000006.11:g.151939275T>G , CM000668.1:g.151939275T>G GRCh37
NC_000006.10:g.151980968T>G NCBI36
NG_021198.1:g.129101T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.2141T>G MANE Select ENSP00000239374.6:p.Leu714Arg
ENST00000239374.7:c.2141T>G ENSP00000239374.6:p.Leu714Arg
NM_025059.3:c.2141T>G NP_079335.2:p.Leu714Arg
XM_011536147.1:c.2159T>G XP_011534449.1:p.Leu720Arg
XM_011536148.1:c.1958T>G XP_011534450.1:p.Leu653Arg
XM_011536147.2:c.2159T>G XP_011534449.1:p.Leu720Arg
XM_011536148.2:c.1958T>G XP_011534450.1:p.Leu653Arg
NM_025059.4:c.2141T>G MANE Select NP_079335.2:p.Leu714Arg