Canonical Allele Identifier: CA2580061249

Gene: DCAF8

Linked Data

• ClinVar Variation Id: 1804868
• ClinVar RCV Id: RCV002470165

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237131T>G , CM000663.2:g.160237131T>G	GRCh38
NC_000001.10:g.160206921T>G , CM000663.1:g.160206921T>G	GRCh37
NC_000001.9:g.158473545T>G	NCBI36
NG_034154.1:g.30430A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.959+4A>C MANE Select	ENSP00000357053.1:n.959+4A>C
ENST00000556710.6:c.*1543+4A>C	ENSP00000451235.2:n.*1543+4A>C
ENST00000647676.1:c.1297+4A>C	ENSP00000497162.1:n.1297+4A>C
ENST00000326837.6:c.959+4A>C	ENSP00000318227.2:n.959+4A>C
ENST00000368073.7:c.959+4A>C	ENSP00000357052.3:n.959+4A>C
ENST00000368074.5:c.959+4A>C	ENSP00000357053.1:n.959+4A>C
ENST00000461888.5:c.959+4A>C	ENSP00000476407.1:n.959+4A>C
ENST00000466253.1:n.474+4A>C
ENST00000556710.5:c.1421+4A>C	ENSP00000451235.1:n.1421+4A>C
NM_015726.3:c.959+4A>C	NP_056541.2:n.959+4A>C
NR_028103.1:n.1471+4A>C
NR_028104.1:n.1397+4A>C
NM_015726.4:c.959+4A>C MANE Select	NP_056541.2:n.959+4A>C
NR_028103.2:n.1492+4A>C
NR_028104.2:n.1418+4A>C