Canonical Allele Identifier: CA820828945
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1349506165

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615653_151615654insT , CM000668.2:g.151615653_151615654insT GRCh38
NC_000006.11:g.151936788_151936789insT , CM000668.1:g.151936788_151936789insT GRCh37
NC_000006.10:g.151978481_151978482insT NCBI36
NG_021198.1:g.126614_126615insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1921_1922insT MANE Select ENSP00000239374.6:p.Glu641ValfsTer?
ENST00000239374.7:c.1921_1922insT ENSP00000239374.6:p.Glu641ValfsTer?
NM_025059.3:c.1921_1922insT NP_079335.2:p.Glu641ValfsTer?
XM_011536147.1:c.1939_1940insT XP_011534449.1:p.Glu647ValfsTer?
XM_011536148.1:c.1738_1739insT XP_011534450.1:p.Glu580ValfsTer?
XM_011536147.2:c.1939_1940insT XP_011534449.1:p.Glu647ValfsTer?
XM_011536148.2:c.1738_1739insT XP_011534450.1:p.Glu580ValfsTer?
XR_001743865.1:n.129+1067_129+1068insA
NM_025059.4:c.1921_1922insT MANE Select NP_079335.2:p.Glu641ValfsTer?