Canonical Allele Identifier: CA2680801618
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618716-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618716G>A , CM000668.2:g.151618716G>A GRCh38
NC_000006.11:g.151939851G>A , CM000668.1:g.151939851G>A GRCh37
NC_000006.10:g.151981544G>A NCBI36
NG_021198.1:g.129677G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*569G>A MANE Select ENSP00000239374.6:n.*569G>A
ENST00000239374.7:c.*569G>A ENSP00000239374.6:n.*569G>A
NM_025059.3:c.*569G>A NP_079335.2:n.*569G>A
XM_011536147.1:c.*569G>A XP_011534449.1:n.*569G>A
XM_011536148.1:c.*569G>A XP_011534450.1:n.*569G>A
XM_011536147.2:c.*569G>A XP_011534449.1:n.*569G>A
XM_011536148.2:c.*569G>A XP_011534450.1:n.*569G>A
NM_025059.4:c.*569G>A MANE Select NP_079335.2:n.*569G>A
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