Canonical Allele Identifier: CA366067673
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151615586-T-A
MyVariant Identifiers: chr6:g.151936721T>A (hg19) chr6:g.151615586T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615586T>A , CM000668.2:g.151615586T>A GRCh38
NC_000006.11:g.151936721T>A , CM000668.1:g.151936721T>A GRCh37
NC_000006.10:g.151978414T>A NCBI36
NG_021198.1:g.126547T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1854T>A MANE Select ENSP00000239374.6:p.Asn618Lys
ENST00000239374.7:c.1854T>A ENSP00000239374.6:p.Asn618Lys
NM_025059.3:c.1854T>A NP_079335.2:p.Asn618Lys
XM_011536147.1:c.1872T>A XP_011534449.1:p.Asn624Lys
XM_011536148.1:c.1671T>A XP_011534450.1:p.Asn557Lys
XM_011536147.2:c.1872T>A XP_011534449.1:p.Asn624Lys
XM_011536148.2:c.1671T>A XP_011534450.1:p.Asn557Lys
XR_001743865.1:n.129+1135A>T
NM_025059.4:c.1854T>A MANE Select NP_079335.2:p.Asn618Lys
Search 100 bp 5'
Search 100 bp 3'