Canonical Allele Identifier: CA1672962785
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1776956024
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615734G>T , CM000668.2:g.151615734G>T GRCh38
NC_000006.11:g.151936869G>T , CM000668.1:g.151936869G>T GRCh37
NC_000006.10:g.151978562G>T NCBI36
NG_021198.1:g.126695G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1947+55G>T MANE Select ENSP00000239374.6:n.1947+55G>T
ENST00000239374.7:c.1947+55G>T ENSP00000239374.6:n.1947+55G>T
NM_025059.3:c.1947+55G>T NP_079335.2:n.1947+55G>T
XM_011536147.1:c.1965+55G>T XP_011534449.1:n.1965+55G>T
XM_011536148.1:c.1764+55G>T XP_011534450.1:n.1764+55G>T
XM_011536147.2:c.1965+55G>T XP_011534449.1:n.1965+55G>T
XM_011536148.2:c.1764+55G>T XP_011534450.1:n.1764+55G>T
XR_001743865.1:n.129+987C>A
NM_025059.4:c.1947+55G>T MANE Select NP_079335.2:n.1947+55G>T
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