Canonical Allele Identifier: CA343222742

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237202-T-C
• MyVariant Identifiers: chr1:g.160206992T>C (hg19) ; chr1:g.160237202T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237202T>C , CM000663.2:g.160237202T>C	GRCh38
NC_000001.10:g.160206992T>C , CM000663.1:g.160206992T>C	GRCh37
NC_000001.9:g.158473616T>C	NCBI36
NG_034154.1:g.30359A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.892A>G MANE Select	ENSP00000357053.1:p.Thr298Ala
ENST00000556710.6:c.*1476A>G	ENSP00000451235.2:n.*1476A>G
ENST00000647676.1:c.1230A>G	ENSP00000497162.1:n.1230A>G
ENST00000326837.6:c.892A>G	ENSP00000318227.2:p.Thr298Ala
ENST00000368073.7:c.892A>G	ENSP00000357052.3:p.Thr298Ala
ENST00000368074.5:c.892A>G	ENSP00000357053.1:p.Thr298Ala
ENST00000461888.5:c.892A>G	ENSP00000476407.1:p.Thr298Ala
ENST00000466253.1:n.407A>G
ENST00000556710.5:c.1354A>G	ENSP00000451235.1:p.Thr452Ala
NM_015726.3:c.892A>G	NP_056541.2:p.Thr298Ala
NR_028103.1:n.1404A>G
NR_028104.1:n.1330A>G
NM_015726.4:c.892A>G MANE Select	NP_056541.2:p.Thr298Ala
NR_028103.2:n.1425A>G
NR_028104.2:n.1351A>G