Canonical Allele Identifier: CA1202237189

Gene: DCAF8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237185A= , CM000663.2:g.160237185A=	GRCh38
NC_000001.10:g.160206975A= , CM000663.1:g.160206975A=	GRCh37
NC_000001.9:g.158473599A=	NCBI36
NG_034154.1:g.30376T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.909T= MANE Select	ENSP00000357053.1:p.Gly303=
ENST00000556710.6:c.*1493T=	ENSP00000451235.2:n.*1493T=
ENST00000647676.1:c.1247T=	ENSP00000497162.1:n.1247T=
ENST00000326837.6:c.909T=	ENSP00000318227.2:p.Gly303=
ENST00000368073.7:c.909T=	ENSP00000357052.3:p.Gly303=
ENST00000368074.5:c.909T=	ENSP00000357053.1:p.Gly303=
ENST00000461888.5:c.909T=	ENSP00000476407.1:p.Gly303=
ENST00000466253.1:n.424T=
ENST00000556710.5:c.1371T=	ENSP00000451235.1:p.Gly457=
NM_015726.3:c.909T=	NP_056541.2:p.Gly303=
NR_028103.1:n.1421T=
NR_028104.1:n.1347T=
NM_015726.4:c.909T= MANE Select	NP_056541.2:p.Gly303=
NR_028103.2:n.1442T=
NR_028104.2:n.1368T=