Canonical Allele Identifier: CA890107548

Gene: DCAF8

Linked Data

• dbSNP Id: rs1358168611
• gnomAD v3: 1-160237052-CAG-C
• gnomAD v4: 1-160237052-CAG-C
• MyVariant Identifiers: chr1:g.160206843_160206844del (hg19) ; chr1:g.160237053_160237054del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237055_160237056del , CM000663.2:g.160237055_160237056del	GRCh38
NC_000001.10:g.160206845_160206846del , CM000663.1:g.160206845_160206846del	GRCh37
NC_000001.9:g.158473469_158473470del	NCBI36
NG_034154.1:g.30507_30508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.959+81_959+82del MANE Select	ENSP00000357053.1:n.959+81_959+82del
ENST00000556710.6:c.*1543+81_*1543+82del	ENSP00000451235.2:n.*1543+81_*1543+82del
ENST00000647676.1:c.1297+81_1297+82del	ENSP00000497162.1:n.1297+81_1297+82del
ENST00000326837.6:c.959+81_959+82del	ENSP00000318227.2:n.959+81_959+82del
ENST00000368073.7:c.959+81_959+82del	ENSP00000357052.3:n.959+81_959+82del
ENST00000368074.5:c.959+81_959+82del	ENSP00000357053.1:n.959+81_959+82del
ENST00000461888.5:c.959+81_959+82del	ENSP00000476407.1:n.959+81_959+82del
ENST00000466253.1:n.474+81_474+82del
ENST00000556710.5:c.1421+81_1421+82del	ENSP00000451235.1:n.1421+81_1421+82del
NM_015726.3:c.959+81_959+82del	NP_056541.2:n.959+81_959+82del
NR_028103.1:n.1471+81_1471+82del
NR_028104.1:n.1397+81_1397+82del
NM_015726.4:c.959+81_959+82del MANE Select	NP_056541.2:n.959+81_959+82del
NR_028103.2:n.1492+81_1492+82del
NR_028104.2:n.1418+81_1418+82del