Canonical Allele Identifier: CA421350949

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237137-C-A
• MyVariant Identifiers: chr1:g.160206927C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237137C>A , CM000663.2:g.160237137C>A	GRCh38
NC_000001.10:g.160206927C>A , CM000663.1:g.160206927C>A	GRCh37
NC_000001.9:g.158473551C>A	NCBI36
NG_034154.1:g.30424G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.957G>T MANE Select	ENSP00000357053.1:p.Ala319=
ENST00000556710.6:c.*1541G>T	ENSP00000451235.2:n.*1541G>T
ENST00000647676.1:c.1295G>T	ENSP00000497162.1:n.1295G>T
ENST00000326837.6:c.957G>T	ENSP00000318227.2:p.Ala319=
ENST00000368073.7:c.957G>T	ENSP00000357052.3:p.Ala319=
ENST00000368074.5:c.957G>T	ENSP00000357053.1:p.Ala319=
ENST00000461888.5:c.957G>T	ENSP00000476407.1:p.Ala319=
ENST00000466253.1:n.472G>T
ENST00000556710.5:c.1419G>T	ENSP00000451235.1:p.Ala473=
NM_015726.3:c.957G>T	NP_056541.2:p.Ala319=
NR_028103.1:n.1469G>T
NR_028104.1:n.1395G>T
NM_015726.4:c.957G>T MANE Select	NP_056541.2:p.Ala319=
NR_028103.2:n.1490G>T
NR_028104.2:n.1416G>T