Canonical Allele Identifier: CA1672947029
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1776363232
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580317G>A , CM000668.2:g.151580317G>A GRCh38
NC_000006.11:g.151901452G>A , CM000668.1:g.151901452G>A GRCh37
NC_000006.10:g.151943145G>A NCBI36
NG_021198.1:g.91278G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5572G>A MANE Select ENSP00000239374.6:n.1093-5572G>A
ENST00000239374.7:c.1093-5572G>A ENSP00000239374.6:n.1093-5572G>A
NM_025059.3:c.1093-5572G>A NP_079335.2:n.1093-5572G>A
XM_011536147.1:c.1111-5572G>A XP_011534449.1:n.1111-5572G>A
XM_011536148.1:c.1110+6826G>A XP_011534450.1:n.1110+6826G>A
XM_011536147.2:c.1111-5572G>A XP_011534449.1:n.1111-5572G>A
XM_011536148.2:c.1110+6826G>A XP_011534450.1:n.1110+6826G>A
NM_025059.4:c.1093-5572G>A MANE Select NP_079335.2:n.1093-5572G>A
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