Canonical Allele Identifier: CA1202237178

Gene: DCAF8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237144C= , CM000663.2:g.160237144C=	GRCh38
NC_000001.10:g.160206934C= , CM000663.1:g.160206934C=	GRCh37
NC_000001.9:g.158473558C=	NCBI36
NG_034154.1:g.30417G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.950G= MANE Select	ENSP00000357053.1:p.Arg317=
ENST00000556710.6:c.*1534G=	ENSP00000451235.2:n.*1534G=
ENST00000647676.1:c.1288G=	ENSP00000497162.1:n.1288G=
ENST00000326837.6:c.950G=	ENSP00000318227.2:p.Arg317=
ENST00000368073.7:c.950G=	ENSP00000357052.3:p.Arg317=
ENST00000368074.5:c.950G=	ENSP00000357053.1:p.Arg317=
ENST00000461888.5:c.950G=	ENSP00000476407.1:p.Arg317=
ENST00000466253.1:n.465G=
ENST00000556710.5:c.1412G=	ENSP00000451235.1:p.Arg471=
NM_015726.3:c.950G=	NP_056541.2:p.Arg317=
NR_028103.1:n.1462G=
NR_028104.1:n.1388G=
NM_015726.4:c.950G= MANE Select	NP_056541.2:p.Arg317=
NR_028103.2:n.1483G=
NR_028104.2:n.1409G=