Canonical Allele Identifier: CA2581611637
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618713-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618713C>G , CM000668.2:g.151618713C>G GRCh38
NC_000006.11:g.151939848C>G , CM000668.1:g.151939848C>G GRCh37
NC_000006.10:g.151981541C>G NCBI36
NG_021198.1:g.129674C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*566C>G MANE Select ENSP00000239374.6:n.*566C>G
ENST00000239374.7:c.*566C>G ENSP00000239374.6:n.*566C>G
NM_025059.3:c.*566C>G NP_079335.2:n.*566C>G
XM_011536147.1:c.*566C>G XP_011534449.1:n.*566C>G
XM_011536148.1:c.*566C>G XP_011534450.1:n.*566C>G
XM_011536147.2:c.*566C>G XP_011534449.1:n.*566C>G
XM_011536148.2:c.*566C>G XP_011534450.1:n.*566C>G
NM_025059.4:c.*566C>G MANE Select NP_079335.2:n.*566C>G
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