Canonical Allele Identifier: CA1202237164

Gene: DCAF8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237116A= , CM000663.2:g.160237116A=	GRCh38
NC_000001.10:g.160206906A= , CM000663.1:g.160206906A=	GRCh37
NC_000001.9:g.158473530A=	NCBI36
NG_034154.1:g.30445T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.959+19T= MANE Select	ENSP00000357053.1:n.959+19T=
ENST00000556710.6:c.*1543+19T=	ENSP00000451235.2:n.*1543+19T=
ENST00000647676.1:c.1297+19T=	ENSP00000497162.1:n.1297+19T=
ENST00000326837.6:c.959+19T=	ENSP00000318227.2:n.959+19T=
ENST00000368073.7:c.959+19T=	ENSP00000357052.3:n.959+19T=
ENST00000368074.5:c.959+19T=	ENSP00000357053.1:n.959+19T=
ENST00000461888.5:c.959+19T=	ENSP00000476407.1:n.959+19T=
ENST00000466253.1:n.474+19T=
ENST00000556710.5:c.1421+19T=	ENSP00000451235.1:n.1421+19T=
NM_015726.3:c.959+19T=	NP_056541.2:n.959+19T=
NR_028103.1:n.1471+19T=
NR_028104.1:n.1397+19T=
NM_015726.4:c.959+19T= MANE Select	NP_056541.2:n.959+19T=
NR_028103.2:n.1492+19T=
NR_028104.2:n.1418+19T=