Canonical Allele Identifier: CA343222955

Gene: DCAF8

Linked Data

• MyVariant Identifiers: chr1:g.160207007G>C (hg19) ; chr1:g.160237217G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237217G>C , CM000663.2:g.160237217G>C	GRCh38
NC_000001.10:g.160207007G>C , CM000663.1:g.160207007G>C	GRCh37
NC_000001.9:g.158473631G>C	NCBI36
NG_034154.1:g.30344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.877C>G MANE Select	ENSP00000357053.1:p.Pro293Ala
ENST00000556710.6:c.*1461C>G	ENSP00000451235.2:n.*1461C>G
ENST00000647676.1:c.1215C>G	ENSP00000497162.1:n.1215C>G
ENST00000326837.6:c.877C>G	ENSP00000318227.2:p.Pro293Ala
ENST00000368073.7:c.877C>G	ENSP00000357052.3:p.Pro293Ala
ENST00000368074.5:c.877C>G	ENSP00000357053.1:p.Pro293Ala
ENST00000461888.5:c.877C>G	ENSP00000476407.1:p.Pro293Ala
ENST00000466253.1:n.392C>G
ENST00000556710.5:c.1339C>G	ENSP00000451235.1:p.Pro447Ala
NM_015726.3:c.877C>G	NP_056541.2:p.Pro293Ala
NR_028103.1:n.1389C>G
NR_028104.1:n.1315C>G
NM_015726.4:c.877C>G MANE Select	NP_056541.2:p.Pro293Ala
NR_028103.2:n.1410C>G
NR_028104.2:n.1336C>G