Canonical Allele Identifier: CA1095894255
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1776880521
gnomAD v3: 6-151612005-G-A
gnomAD v4: 6-151612005-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151612005G>A , CM000668.2:g.151612005G>A GRCh38
NC_000006.11:g.151933140G>A , CM000668.1:g.151933140G>A GRCh37
NC_000006.10:g.151974833G>A NCBI36
NG_021198.1:g.122966G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1711-3438G>A MANE Select ENSP00000239374.6:n.1711-3438G>A
ENST00000239374.7:c.1711-3438G>A ENSP00000239374.6:n.1711-3438G>A
ENST00000537358.1:n.497-3438G>A
NM_025059.3:c.1711-3438G>A NP_079335.2:n.1711-3438G>A
XM_011536147.1:c.1729-3438G>A XP_011534449.1:n.1729-3438G>A
XM_011536148.1:c.1528-3438G>A XP_011534450.1:n.1528-3438G>A
XM_011536147.2:c.1729-3438G>A XP_011534449.1:n.1729-3438G>A
XM_011536148.2:c.1528-3438G>A XP_011534450.1:n.1528-3438G>A
XR_001743865.1:n.130-733C>T
NM_025059.4:c.1711-3438G>A MANE Select NP_079335.2:n.1711-3438G>A
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