Canonical Allele Identifier: CA1202237173

Gene: DCAF8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237135G= , CM000663.2:g.160237135G=	GRCh38
NC_000001.10:g.160206925G= , CM000663.1:g.160206925G=	GRCh37
NC_000001.9:g.158473549G=	NCBI36
NG_034154.1:g.30426C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.959C= MANE Select	ENSP00000357053.1:p.Ser320=
ENST00000556710.6:c.*1543C=	ENSP00000451235.2:n.*1543C=
ENST00000647676.1:c.1297C=	ENSP00000497162.1:n.1297C=
ENST00000326837.6:c.959C=	ENSP00000318227.2:p.Ser320=
ENST00000368073.7:c.959C=	ENSP00000357052.3:p.Ser320=
ENST00000368074.5:c.959C=	ENSP00000357053.1:p.Ser320=
ENST00000461888.5:c.959C=	ENSP00000476407.1:p.Ser320=
ENST00000466253.1:n.474C=
ENST00000556710.5:c.1421C=	ENSP00000451235.1:p.Ser474=
NM_015726.3:c.959C=	NP_056541.2:p.Ser320=
NR_028103.1:n.1471C=
NR_028104.1:n.1397C=
NM_015726.4:c.959C= MANE Select	NP_056541.2:p.Ser320=
NR_028103.2:n.1492C=
NR_028104.2:n.1418C=