Canonical Allele Identifier: CA421350958

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237140-T-C
• COSMIC: COSM2085414 ; COSM2085415
• MyVariant Identifiers: chr1:g.160206930T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237140T>C , CM000663.2:g.160237140T>C	GRCh38
NC_000001.10:g.160206930T>C , CM000663.1:g.160206930T>C	GRCh37
NC_000001.9:g.158473554T>C	NCBI36
NG_034154.1:g.30421A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.954A>G MANE Select	ENSP00000357053.1:p.Pro318=
ENST00000556710.6:c.*1538A>G	ENSP00000451235.2:n.*1538A>G
ENST00000647676.1:c.1292A>G	ENSP00000497162.1:n.1292A>G
ENST00000326837.6:c.954A>G	ENSP00000318227.2:p.Pro318=
ENST00000368073.7:c.954A>G	ENSP00000357052.3:p.Pro318=
ENST00000368074.5:c.954A>G	ENSP00000357053.1:p.Pro318=
ENST00000461888.5:c.954A>G	ENSP00000476407.1:p.Pro318=
ENST00000466253.1:n.469A>G
ENST00000556710.5:c.1416A>G	ENSP00000451235.1:p.Pro472=
NM_015726.3:c.954A>G	NP_056541.2:p.Pro318=
NR_028103.1:n.1466A>G
NR_028104.1:n.1392A>G
NM_015726.4:c.954A>G MANE Select	NP_056541.2:p.Pro318=
NR_028103.2:n.1487A>G
NR_028104.2:n.1413A>G