Canonical Allele Identifier: CA421351152

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237221-C-T
• MyVariant Identifiers: chr1:g.160207011C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237221C>T , CM000663.2:g.160237221C>T	GRCh38
NC_000001.10:g.160207011C>T , CM000663.1:g.160207011C>T	GRCh37
NC_000001.9:g.158473635C>T	NCBI36
NG_034154.1:g.30340G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.873G>A MANE Select	ENSP00000357053.1:p.Leu291=
ENST00000556710.6:c.*1457G>A	ENSP00000451235.2:n.*1457G>A
ENST00000647676.1:c.1211G>A	ENSP00000497162.1:n.1211G>A
ENST00000326837.6:c.873G>A	ENSP00000318227.2:p.Leu291=
ENST00000368073.7:c.873G>A	ENSP00000357052.3:p.Leu291=
ENST00000368074.5:c.873G>A	ENSP00000357053.1:p.Leu291=
ENST00000461888.5:c.873G>A	ENSP00000476407.1:p.Leu291=
ENST00000466253.1:n.388G>A
ENST00000556710.5:c.1335G>A	ENSP00000451235.1:p.Leu445=
NM_015726.3:c.873G>A	NP_056541.2:p.Leu291=
NR_028103.1:n.1385G>A
NR_028104.1:n.1311G>A
NM_015726.4:c.873G>A MANE Select	NP_056541.2:p.Leu291=
NR_028103.2:n.1406G>A
NR_028104.2:n.1332G>A