Canonical Allele Identifier: CA343222224

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237151-G-C
• MyVariant Identifiers: chr1:g.160206941G>C (hg19) ; chr1:g.160237151G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237151G>C , CM000663.2:g.160237151G>C	GRCh38
NC_000001.10:g.160206941G>C , CM000663.1:g.160206941G>C	GRCh37
NC_000001.9:g.158473565G>C	NCBI36
NG_034154.1:g.30410C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.943C>G MANE Select	ENSP00000357053.1:p.Gln315Glu
ENST00000556710.6:c.*1527C>G	ENSP00000451235.2:n.*1527C>G
ENST00000647676.1:c.1281C>G	ENSP00000497162.1:n.1281C>G
ENST00000326837.6:c.943C>G	ENSP00000318227.2:p.Gln315Glu
ENST00000368073.7:c.943C>G	ENSP00000357052.3:p.Gln315Glu
ENST00000368074.5:c.943C>G	ENSP00000357053.1:p.Gln315Glu
ENST00000461888.5:c.943C>G	ENSP00000476407.1:p.Gln315Glu
ENST00000466253.1:n.458C>G
ENST00000556710.5:c.1405C>G	ENSP00000451235.1:p.Gln469Glu
NM_015726.3:c.943C>G	NP_056541.2:p.Gln315Glu
NR_028103.1:n.1455C>G
NR_028104.1:n.1381C>G
NM_015726.4:c.943C>G MANE Select	NP_056541.2:p.Gln315Glu
NR_028103.2:n.1476C>G
NR_028104.2:n.1402C>G