Canonical Allele Identifier: CA2680801176
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618252-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618252G>A , CM000668.2:g.151618252G>A GRCh38
NC_000006.11:g.151939387G>A , CM000668.1:g.151939387G>A GRCh37
NC_000006.10:g.151981080G>A NCBI36
NG_021198.1:g.129213G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*105G>A MANE Select ENSP00000239374.6:n.*105G>A
ENST00000239374.7:c.*105G>A ENSP00000239374.6:n.*105G>A
NM_025059.3:c.*105G>A NP_079335.2:n.*105G>A
XM_011536147.1:c.*105G>A XP_011534449.1:n.*105G>A
XM_011536148.1:c.*105G>A XP_011534450.1:n.*105G>A
XM_011536147.2:c.*105G>A XP_011534449.1:n.*105G>A
XM_011536148.2:c.*105G>A XP_011534450.1:n.*105G>A
NM_025059.4:c.*105G>A MANE Select NP_079335.2:n.*105G>A
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