Canonical Allele Identifier: CA1672946971
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs11155797

Genomic Alleles

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

Transcript Alleles

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