Canonical Allele Identifier: CA2648660565

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237027-G-GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237030_160237031dup , CM000663.2:g.160237030_160237031dup	GRCh38
NC_000001.10:g.160206820_160206821dup , CM000663.1:g.160206820_160206821dup	GRCh37
NC_000001.9:g.158473444_158473445dup	NCBI36
NG_034154.1:g.30532_30533dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.959+106_959+107dup MANE Select	ENSP00000357053.1:n.959+106_959+107dup
ENST00000556710.6:c.*1543+106_*1543+107dup	ENSP00000451235.2:n.*1543+106_*1543+107dup
ENST00000647676.1:c.1297+106_1297+107dup	ENSP00000497162.1:n.1297+106_1297+107dup
ENST00000326837.6:c.959+106_959+107dup	ENSP00000318227.2:n.959+106_959+107dup
ENST00000368073.7:c.959+106_959+107dup	ENSP00000357052.3:n.959+106_959+107dup
ENST00000368074.5:c.959+106_959+107dup	ENSP00000357053.1:n.959+106_959+107dup
ENST00000461888.5:c.959+106_959+107dup	ENSP00000476407.1:n.959+106_959+107dup
ENST00000466253.1:n.474+106_474+107dup
ENST00000556710.5:c.1421+106_1421+107dup	ENSP00000451235.1:n.1421+106_1421+107dup
NM_015726.3:c.959+106_959+107dup	NP_056541.2:n.959+106_959+107dup
NR_028103.1:n.1471+106_1471+107dup
NR_028104.1:n.1397+106_1397+107dup
NM_015726.4:c.959+106_959+107dup MANE Select	NP_056541.2:n.959+106_959+107dup
NR_028103.2:n.1492+106_1492+107dup
NR_028104.2:n.1418+106_1418+107dup