Canonical Allele Identifier: CA366069786
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151939266T>C (hg19) chr6:g.151618131T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618131T>C , CM000668.2:g.151618131T>C GRCh38
NC_000006.11:g.151939266T>C , CM000668.1:g.151939266T>C GRCh37
NC_000006.10:g.151980959T>C NCBI36
NG_021198.1:g.129092T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.2132T>C MANE Select ENSP00000239374.6:p.Leu711Ser
ENST00000239374.7:c.2132T>C ENSP00000239374.6:p.Leu711Ser
NM_025059.3:c.2132T>C NP_079335.2:p.Leu711Ser
XM_011536147.1:c.2150T>C XP_011534449.1:p.Leu717Ser
XM_011536148.1:c.1949T>C XP_011534450.1:p.Leu650Ser
XM_011536147.2:c.2150T>C XP_011534449.1:p.Leu717Ser
XM_011536148.2:c.1949T>C XP_011534450.1:p.Leu650Ser
NM_025059.4:c.2132T>C MANE Select NP_079335.2:p.Leu711Ser
Search 100 bp 5'
Search 100 bp 3'