Canonical Allele Identifier: CA2869768
Gene: DCAF16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17803759A>G , CM000666.2:g.17803759A>G GRCh38
NC_000004.11:g.17805382A>G , CM000666.1:g.17805382A>G GRCh37
NC_000004.10:g.17414480A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_017741.4:c.383T>C MANE Select NP_060211.3:p.Leu128Pro
ENST00000382247.6:c.383T>C MANE Select ENSP00000371682.1:p.Leu128Pro
NM_001345880.1:c.383T>C NP_001332809.1:p.Leu128Pro
NM_001345880.2:c.383T>C NP_001332809.1:p.Leu128Pro
NM_001345881.1:c.383T>C NP_001332810.1:p.Leu128Pro
NM_001345881.2:c.383T>C NP_001332810.1:p.Leu128Pro
NM_001345882.1:c.383T>C NP_001332811.1:p.Leu128Pro
NM_001345882.2:c.383T>C NP_001332811.1:p.Leu128Pro
NM_001345884.1:c.383T>C NP_001332813.1:p.Leu128Pro
NM_001345884.2:c.383T>C NP_001332813.1:p.Leu128Pro
NM_001345885.1:c.383T>C NP_001332814.1:p.Leu128Pro
NM_001345885.2:c.383T>C NP_001332814.1:p.Leu128Pro
NM_017741.3:c.383T>C NP_060211.3:p.Leu128Pro
NR_144301.1:n.799+645T>C
NR_144301.2:n.798+645T>C
NR_144303.1:n.680+645T>C
NR_144303.2:n.679+645T>C
NR_144305.1:n.665+645T>C
NR_144305.2:n.664+645T>C
NR_144310.1:n.784+645T>C
NR_144310.2:n.783+645T>C
ENST00000382247.5:c.383T>C ENSP00000371682.1:p.Leu128Pro
XM_005248169.2:c.383T>C XP_005248226.1:p.Leu128Pro
XM_005248170.2:c.383T>C XP_005248227.1:p.Leu128Pro
XM_005248171.2:c.383T>C XP_005248228.1:p.Leu128Pro
XM_006713966.2:c.383T>C XP_006714029.1:p.Leu128Pro
XM_011513849.1:c.383T>C XP_011512151.1:p.Leu128Pro
XM_024454104.1:c.383T>C XP_024309872.1:p.Leu128Pro