Canonical Allele Identifier: CA2581611335
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580202C>A , CM000668.2:g.151580202C>A GRCh38
NC_000006.11:g.151901337C>A , CM000668.1:g.151901337C>A GRCh37
NC_000006.10:g.151943030C>A NCBI36
NG_021198.1:g.91163C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5687C>A MANE Select ENSP00000239374.6:n.1093-5687C>A
ENST00000239374.7:c.1093-5687C>A ENSP00000239374.6:n.1093-5687C>A
NM_025059.3:c.1093-5687C>A NP_079335.2:n.1093-5687C>A
XM_011536147.1:c.1111-5687C>A XP_011534449.1:n.1111-5687C>A
XM_011536148.1:c.1110+6711C>A XP_011534450.1:n.1110+6711C>A
XM_011536147.2:c.1111-5687C>A XP_011534449.1:n.1111-5687C>A
XM_011536148.2:c.1110+6711C>A XP_011534450.1:n.1110+6711C>A
NM_025059.4:c.1093-5687C>A MANE Select NP_079335.2:n.1093-5687C>A
Search 100 bp 5'
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