Canonical Allele Identifier: CA2680801492
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618614-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618614G>T , CM000668.2:g.151618614G>T GRCh38
NC_000006.11:g.151939749G>T , CM000668.1:g.151939749G>T GRCh37
NC_000006.10:g.151981442G>T NCBI36
NG_021198.1:g.129575G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*467G>T MANE Select ENSP00000239374.6:n.*467G>T
ENST00000239374.7:c.*467G>T ENSP00000239374.6:n.*467G>T
NM_025059.3:c.*467G>T NP_079335.2:n.*467G>T
XM_011536147.1:c.*467G>T XP_011534449.1:n.*467G>T
XM_011536148.1:c.*467G>T XP_011534450.1:n.*467G>T
XM_011536147.2:c.*467G>T XP_011534449.1:n.*467G>T
XM_011536148.2:c.*467G>T XP_011534450.1:n.*467G>T
NM_025059.4:c.*467G>T MANE Select NP_079335.2:n.*467G>T
Search 100 bp 5'
Search 100 bp 3'