Canonical Allele Identifier: CA343222390

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237171-A-C
• MyVariant Identifiers: chr1:g.160206961A>C (hg19) ; chr1:g.160237171A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237171A>C , CM000663.2:g.160237171A>C	GRCh38
NC_000001.10:g.160206961A>C , CM000663.1:g.160206961A>C	GRCh37
NC_000001.9:g.158473585A>C	NCBI36
NG_034154.1:g.30390T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.923T>G MANE Select	ENSP00000357053.1:p.Val308Gly
ENST00000556710.6:c.*1507T>G	ENSP00000451235.2:n.*1507T>G
ENST00000647676.1:c.1261T>G	ENSP00000497162.1:n.1261T>G
ENST00000326837.6:c.923T>G	ENSP00000318227.2:p.Val308Gly
ENST00000368073.7:c.923T>G	ENSP00000357052.3:p.Val308Gly
ENST00000368074.5:c.923T>G	ENSP00000357053.1:p.Val308Gly
ENST00000461888.5:c.923T>G	ENSP00000476407.1:p.Val308Gly
ENST00000466253.1:n.438T>G
ENST00000556710.5:c.1385T>G	ENSP00000451235.1:p.Val462Gly
NM_015726.3:c.923T>G	NP_056541.2:p.Val308Gly
NR_028103.1:n.1435T>G
NR_028104.1:n.1361T>G
NM_015726.4:c.923T>G MANE Select	NP_056541.2:p.Val308Gly
NR_028103.2:n.1456T>G
NR_028104.2:n.1382T>G