Canonical Allele Identifier: CA820809487
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1468918393
MyVariant Identifiers: chr6:g.151901301_151901310del (hg19) chr6:g.151580166_151580175del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580169_151580178del , CM000668.2:g.151580169_151580178del GRCh38
NC_000006.11:g.151901304_151901313del , CM000668.1:g.151901304_151901313del GRCh37
NC_000006.10:g.151942997_151943006del NCBI36
NG_021198.1:g.91130_91139del

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5720_1093-5711del MANE Select ENSP00000239374.6:n.1093-5720_1093-5711de...
ENST00000239374.7:c.1093-5720_1093-5711del ENSP00000239374.6:n.1093-5720_1093-5711de...
NM_025059.3:c.1093-5720_1093-5711del NP_079335.2:n.1093-5720_1093-5711del
XM_011536147.1:c.1111-5720_1111-5711del XP_011534449.1:n.1111-5720_1111-5711del
XM_011536148.1:c.1110+6678_1110+6687del XP_011534450.1:n.1110+6678_1110+6687del
XM_011536147.2:c.1111-5720_1111-5711del XP_011534449.1:n.1111-5720_1111-5711del
XM_011536148.2:c.1110+6678_1110+6687del XP_011534450.1:n.1110+6678_1110+6687del
NM_025059.4:c.1093-5720_1093-5711del MANE Select NP_079335.2:n.1093-5720_1093-5711del
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