Canonical Allele Identifier: CA1202237139

Gene: DCAF8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237052_160237054delinsCAG , CM000663.2:g.160237052_160237054delinsCAG	GRCh38
NC_000001.10:g.160206842_160206844delinsCAG , CM000663.1:g.160206842_160206844delinsCAG	GRCh37
NC_000001.9:g.158473466_158473468delinsCAG	NCBI36
NG_034154.1:g.30507_30509delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.959+81_959+83delinsCTG MANE Select	ENSP00000357053.1:n.959+81_959+83delinsCTG
ENST00000556710.6:c.*1543+81_*1543+83delinsCTG	ENSP00000451235.2:n.*1543+81_*1543+83delinsCTG
ENST00000647676.1:c.1297+81_1297+83delinsCTG	ENSP00000497162.1:n.1297+81_1297+83delinsCTG
ENST00000326837.6:c.959+81_959+83delinsCTG	ENSP00000318227.2:n.959+81_959+83delinsCTG
ENST00000368073.7:c.959+81_959+83delinsCTG	ENSP00000357052.3:n.959+81_959+83delinsCTG
ENST00000368074.5:c.959+81_959+83delinsCTG	ENSP00000357053.1:n.959+81_959+83delinsCTG
ENST00000461888.5:c.959+81_959+83delinsCTG	ENSP00000476407.1:n.959+81_959+83delinsCTG
ENST00000466253.1:n.474+81_474+83delinsCTG
ENST00000556710.5:c.1421+81_1421+83delinsCTG	ENSP00000451235.1:n.1421+81_1421+83delinsCTG
NM_015726.3:c.959+81_959+83delinsCTG	NP_056541.2:n.959+81_959+83delinsCTG
NR_028103.1:n.1471+81_1471+83delinsCTG
NR_028104.1:n.1397+81_1397+83delinsCTG
NM_015726.4:c.959+81_959+83delinsCTG MANE Select	NP_056541.2:n.959+81_959+83delinsCTG
NR_028103.2:n.1492+81_1492+83delinsCTG
NR_028104.2:n.1418+81_1418+83delinsCTG