Canonical Allele Identifier: CA2680801510
Gene: CCDC170 HGNC NCBI

Linked Data

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

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

Transcript Alleles

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