Canonical Allele Identifier: CA343222685

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237197-G-T
• MyVariant Identifiers: chr1:g.160206987G>T (hg19) ; chr1:g.160237197G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237197G>T , CM000663.2:g.160237197G>T	GRCh38
NC_000001.10:g.160206987G>T , CM000663.1:g.160206987G>T	GRCh37
NC_000001.9:g.158473611G>T	NCBI36
NG_034154.1:g.30364C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.897C>A MANE Select	ENSP00000357053.1:p.Phe299Leu
ENST00000556710.6:c.*1481C>A	ENSP00000451235.2:n.*1481C>A
ENST00000647676.1:c.1235C>A	ENSP00000497162.1:n.1235C>A
ENST00000326837.6:c.897C>A	ENSP00000318227.2:p.Phe299Leu
ENST00000368073.7:c.897C>A	ENSP00000357052.3:p.Phe299Leu
ENST00000368074.5:c.897C>A	ENSP00000357053.1:p.Phe299Leu
ENST00000461888.5:c.897C>A	ENSP00000476407.1:p.Phe299Leu
ENST00000466253.1:n.412C>A
ENST00000556710.5:c.1359C>A	ENSP00000451235.1:p.Phe453Leu
NM_015726.3:c.897C>A	NP_056541.2:p.Phe299Leu
NR_028103.1:n.1409C>A
NR_028104.1:n.1335C>A
NM_015726.4:c.897C>A MANE Select	NP_056541.2:p.Phe299Leu
NR_028103.2:n.1430C>A
NR_028104.2:n.1356C>A