Canonical Allele Identifier: CA343222250

Gene: DCAF8

Linked Data

• MyVariant Identifiers: chr1:g.160206943C>T (hg19) ; chr1:g.160237153C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237153C>T , CM000663.2:g.160237153C>T	GRCh38
NC_000001.10:g.160206943C>T , CM000663.1:g.160206943C>T	GRCh37
NC_000001.9:g.158473567C>T	NCBI36
NG_034154.1:g.30408G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.941G>A MANE Select	ENSP00000357053.1:p.Arg314Lys
ENST00000556710.6:c.*1525G>A	ENSP00000451235.2:n.*1525G>A
ENST00000647676.1:c.1279G>A	ENSP00000497162.1:n.1279G>A
ENST00000326837.6:c.941G>A	ENSP00000318227.2:p.Arg314Lys
ENST00000368073.7:c.941G>A	ENSP00000357052.3:p.Arg314Lys
ENST00000368074.5:c.941G>A	ENSP00000357053.1:p.Arg314Lys
ENST00000461888.5:c.941G>A	ENSP00000476407.1:p.Arg314Lys
ENST00000466253.1:n.456G>A
ENST00000556710.5:c.1403G>A	ENSP00000451235.1:p.Arg468Lys
NM_015726.3:c.941G>A	NP_056541.2:p.Arg314Lys
NR_028103.1:n.1453G>A
NR_028104.1:n.1379G>A
NM_015726.4:c.941G>A MANE Select	NP_056541.2:p.Arg314Lys
NR_028103.2:n.1474G>A
NR_028104.2:n.1400G>A