Canonical Allele Identifier: CA389231316

Gene: DCAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24120980T>C , CM000676.2:g.24120980T>C	GRCh38
NC_000014.8:g.24590189T>C , CM000676.1:g.24590189T>C	GRCh37
NC_000014.7:g.23660029T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025230.5:c.1235T>C MANE Select	NP_079506.3:p.Val412Ala
ENST00000446197.8:c.1235T>C MANE Select	ENSP00000415556.4:p.Val412Ala
NM_001163484.1:c.1235T>C	NP_001156956.1:p.Val412Ala
NM_001163484.2:c.1235T>C	NP_001156956.1:p.Val412Ala
NM_025230.4:c.1235T>C	NP_079506.3:p.Val412Ala
NM_181357.2:c.1157T>C	NP_852002.1:p.Val386Ala
NR_028099.1:n.1877T>C
NR_028099.2:n.1877T>C
NR_028100.1:n.1492T>C
ENST00000326009.9:c.*996T>C	ENSP00000323680.5:n.*996T>C
ENST00000396936.5:c.935T>C	ENSP00000380142.1:p.Val312Ala
ENST00000396941.8:c.1157T>C	ENSP00000380146.4:p.Val386Ala
ENST00000446197.7:c.1235T>C	ENSP00000415556.3:p.Val412Ala
ENST00000557802.5:c.*931T>C	ENSP00000453462.1:n.*931T>C
ENST00000558325.2:c.25T>C
ENST00000558624.1:n.1403T>C
ENST00000558914.5:c.*766T>C	ENSP00000453035.1:n.*766T>C
ENST00000559115.5:c.1235T>C	ENSP00000452898.1:p.Val412Ala
ENST00000559144.1:c.455T>C	ENSP00000453115.1:p.Val152Ala
ENST00000559472.1:n.22T>C