Canonical Allele Identifier: CA16042299

Gene: DCAF8

Linked Data

• ClinVar Variation Id: 373149
• ClinVar RCV Id: RCV000413871
• dbSNP Id: rs1057518253
• MyVariant Identifiers: chr1:g.160210058G>A (hg19) ; chr1:g.160240268G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160240268G>A , CM000663.2:g.160240268G>A	GRCh38
NC_000001.10:g.160210058G>A , CM000663.1:g.160210058G>A	GRCh37
NC_000001.9:g.158476682G>A	NCBI36
NG_034154.1:g.27293C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.152C>T MANE Select	ENSP00000357053.1:p.Thr51Ile
ENST00000556710.6:c.*736C>T	ENSP00000451235.2:n.*736C>T
ENST00000647676.1:c.490C>T	ENSP00000497162.1:n.490C>T
ENST00000326837.6:c.152C>T	ENSP00000318227.2:p.Thr51Ile
ENST00000368073.7:c.152C>T	ENSP00000357052.3:p.Thr51Ile
ENST00000368074.5:c.152C>T	ENSP00000357053.1:p.Thr51Ile
ENST00000407642.6:c.152C>T	ENSP00000384118.2:p.Thr51Ile
ENST00000440682.5:c.152C>T	ENSP00000411875.1:p.Thr51Ile
ENST00000447377.5:c.152C>T	ENSP00000413688.1:p.Thr51Ile
ENST00000461888.5:c.152C>T	ENSP00000476407.1:p.Thr51Ile
ENST00000475733.5:c.152C>T	ENSP00000476351.1:p.Thr51Ile
ENST00000485079.1:c.788C>T	ENSP00000450870.1:p.Thr263Ile
ENST00000495887.1:c.77C>T	ENSP00000477012.1:p.Thr26Ile
ENST00000556710.5:c.614C>T	ENSP00000451235.1:p.Thr205Ile
ENST00000610139.5:c.152C>T	ENSP00000477464.1:p.Thr51Ile
NM_015726.3:c.152C>T	NP_056541.2:p.Thr51Ile
NR_028103.1:n.664C>T
NR_028104.1:n.590C>T
NR_028105.1:n.664C>T
NR_028106.1:n.431C>T
NM_015726.4:c.152C>T MANE Select	NP_056541.2:p.Thr51Ile
NR_028103.2:n.685C>T
NR_028104.2:n.611C>T
NR_028105.2:n.685C>T
NR_028106.2:n.493C>T