Canonical Allele Identifier: CA1672946981
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1583035843
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580221C>A , CM000668.2:g.151580221C>A GRCh38
NC_000006.11:g.151901356C>A , CM000668.1:g.151901356C>A GRCh37
NC_000006.10:g.151943049C>A NCBI36
NG_021198.1:g.91182C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5668C>A MANE Select ENSP00000239374.6:n.1093-5668C>A
ENST00000239374.7:c.1093-5668C>A ENSP00000239374.6:n.1093-5668C>A
NM_025059.3:c.1093-5668C>A NP_079335.2:n.1093-5668C>A
XM_011536147.1:c.1111-5668C>A XP_011534449.1:n.1111-5668C>A
XM_011536148.1:c.1110+6730C>A XP_011534450.1:n.1110+6730C>A
XM_011536147.2:c.1111-5668C>A XP_011534449.1:n.1111-5668C>A
XM_011536148.2:c.1110+6730C>A XP_011534450.1:n.1110+6730C>A
NM_025059.4:c.1093-5668C>A MANE Select NP_079335.2:n.1093-5668C>A
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