Canonical Allele Identifier: CA1095897080
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1777011273
gnomAD v3: 6-151618730-G-A
gnomAD v4: 6-151618730-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618730G>A , CM000668.2:g.151618730G>A GRCh38
NC_000006.11:g.151939865G>A , CM000668.1:g.151939865G>A GRCh37
NC_000006.10:g.151981558G>A NCBI36
NG_021198.1:g.129691G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*583G>A MANE Select ENSP00000239374.6:n.*583G>A
ENST00000239374.7:c.*583G>A ENSP00000239374.6:n.*583G>A
NM_025059.3:c.*583G>A NP_079335.2:n.*583G>A
XM_011536147.1:c.*583G>A XP_011534449.1:n.*583G>A
XM_011536148.1:c.*583G>A XP_011534450.1:n.*583G>A
XM_011536147.2:c.*583G>A XP_011534449.1:n.*583G>A
XM_011536148.2:c.*583G>A XP_011534450.1:n.*583G>A
NM_025059.4:c.*583G>A MANE Select NP_079335.2:n.*583G>A
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