Canonical Allele Identifier: CA343223046

Gene: DCAF8

Linked Data

• gnomAD v4: 1-160237228-A-G
• MyVariant Identifiers: chr1:g.160207018A>G (hg19) ; chr1:g.160237228A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160237228A>G , CM000663.2:g.160237228A>G	GRCh38
NC_000001.10:g.160207018A>G , CM000663.1:g.160207018A>G	GRCh37
NC_000001.9:g.158473642A>G	NCBI36
NG_034154.1:g.30333T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368074.6:c.866T>C MANE Select	ENSP00000357053.1:p.Leu289Ser
ENST00000556710.6:c.*1450T>C	ENSP00000451235.2:n.*1450T>C
ENST00000647676.1:c.1204T>C	ENSP00000497162.1:n.1204T>C
ENST00000326837.6:c.866T>C	ENSP00000318227.2:p.Leu289Ser
ENST00000368073.7:c.866T>C	ENSP00000357052.3:p.Leu289Ser
ENST00000368074.5:c.866T>C	ENSP00000357053.1:p.Leu289Ser
ENST00000461888.5:c.866T>C	ENSP00000476407.1:p.Leu289Ser
ENST00000466253.1:n.381T>C
ENST00000556710.5:c.1328T>C	ENSP00000451235.1:p.Leu443Ser
NM_015726.3:c.866T>C	NP_056541.2:p.Leu289Ser
NR_028103.1:n.1378T>C
NR_028104.1:n.1304T>C
NM_015726.4:c.866T>C MANE Select	NP_056541.2:p.Leu289Ser
NR_028103.2:n.1399T>C
NR_028104.2:n.1325T>C