Canonical Allele Identifier: CA2680801509
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618625-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618625T>G , CM000668.2:g.151618625T>G GRCh38
NC_000006.11:g.151939760T>G , CM000668.1:g.151939760T>G GRCh37
NC_000006.10:g.151981453T>G NCBI36
NG_021198.1:g.129586T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*478T>G MANE Select ENSP00000239374.6:n.*478T>G
ENST00000239374.7:c.*478T>G ENSP00000239374.6:n.*478T>G
NM_025059.3:c.*478T>G NP_079335.2:n.*478T>G
XM_011536147.1:c.*478T>G XP_011534449.1:n.*478T>G
XM_011536148.1:c.*478T>G XP_011534450.1:n.*478T>G
XM_011536147.2:c.*478T>G XP_011534449.1:n.*478T>G
XM_011536148.2:c.*478T>G XP_011534450.1:n.*478T>G
NM_025059.4:c.*478T>G MANE Select NP_079335.2:n.*478T>G
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