Canonical Allele Identifier: CA2680801501
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618619-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618619A>T , CM000668.2:g.151618619A>T GRCh38
NC_000006.11:g.151939754A>T , CM000668.1:g.151939754A>T GRCh37
NC_000006.10:g.151981447A>T NCBI36
NG_021198.1:g.129580A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*472A>T MANE Select ENSP00000239374.6:n.*472A>T
ENST00000239374.7:c.*472A>T ENSP00000239374.6:n.*472A>T
NM_025059.3:c.*472A>T NP_079335.2:n.*472A>T
XM_011536147.1:c.*472A>T XP_011534449.1:n.*472A>T
XM_011536148.1:c.*472A>T XP_011534450.1:n.*472A>T
XM_011536147.2:c.*472A>T XP_011534449.1:n.*472A>T
XM_011536148.2:c.*472A>T XP_011534450.1:n.*472A>T
NM_025059.4:c.*472A>T MANE Select NP_079335.2:n.*472A>T
Search 100 bp 5'
Search 100 bp 3'