Canonical Allele Identifier: CA366067589
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615579A>T , CM000668.2:g.151615579A>T GRCh38
NC_000006.11:g.151936714A>T , CM000668.1:g.151936714A>T GRCh37
NC_000006.10:g.151978407A>T NCBI36
NG_021198.1:g.126540A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1847A>T MANE Select ENSP00000239374.6:p.Lys616Met
ENST00000239374.7:c.1847A>T ENSP00000239374.6:p.Lys616Met
NM_025059.3:c.1847A>T NP_079335.2:p.Lys616Met
XM_011536147.1:c.1865A>T XP_011534449.1:p.Lys622Met
XM_011536148.1:c.1664A>T XP_011534450.1:p.Lys555Met
XM_011536147.2:c.1865A>T XP_011534449.1:p.Lys622Met
XM_011536148.2:c.1664A>T XP_011534450.1:p.Lys555Met
XR_001743865.1:n.129+1142T>A
NM_025059.4:c.1847A>T MANE Select NP_079335.2:p.Lys616Met