Canonical Allele Identifier: CA421350975

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237146-G-A
• MyVariant Identifiers: chr1:g.160206936G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237146G>A , CM000663.2:g.160237146G>A	GRCh38
NC_000001.10:g.160206936G>A , CM000663.1:g.160206936G>A	GRCh37
NC_000001.9:g.158473560G>A	NCBI36
NG_034154.1:g.30415C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.948C>T MANE Select	ENSP00000357053.1:p.Asp316=
ENST00000556710.6:c.*1532C>T	ENSP00000451235.2:n.*1532C>T
ENST00000647676.1:c.1286C>T	ENSP00000497162.1:n.1286C>T
ENST00000326837.6:c.948C>T	ENSP00000318227.2:p.Asp316=
ENST00000368073.7:c.948C>T	ENSP00000357052.3:p.Asp316=
ENST00000368074.5:c.948C>T	ENSP00000357053.1:p.Asp316=
ENST00000461888.5:c.948C>T	ENSP00000476407.1:p.Asp316=
ENST00000466253.1:n.463C>T
ENST00000556710.5:c.1410C>T	ENSP00000451235.1:p.Asp470=
NM_015726.3:c.948C>T	NP_056541.2:p.Asp316=
NR_028103.1:n.1460C>T
NR_028104.1:n.1386C>T
NM_015726.4:c.948C>T MANE Select	NP_056541.2:p.Asp316=
NR_028103.2:n.1481C>T
NR_028104.2:n.1407C>T