Canonical Allele Identifier: CA2869750

Gene: DCAF16

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17803664T>G , CM000666.2:g.17803664T>G	GRCh38
NC_000004.11:g.17805287T>G , CM000666.1:g.17805287T>G	GRCh37
NC_000004.10:g.17414385T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382247.6:c.478A>C MANE Select	ENSP00000371682.1:p.Thr160Pro
ENST00000382247.5:c.478A>C	ENSP00000371682.1:p.Thr160Pro
NM_017741.3:c.478A>C	NP_060211.3:p.Thr160Pro
XM_005248169.2:c.478A>C	XP_005248226.1:p.Thr160Pro
XM_005248170.2:c.478A>C	XP_005248227.1:p.Thr160Pro
XM_005248171.2:c.478A>C	XP_005248228.1:p.Thr160Pro
XM_006713966.2:c.478A>C	XP_006714029.1:p.Thr160Pro
XM_011513849.1:c.478A>C	XP_011512151.1:p.Thr160Pro
NM_001345880.1:c.478A>C	NP_001332809.1:p.Thr160Pro
NM_001345881.1:c.478A>C	NP_001332810.1:p.Thr160Pro
NM_001345882.1:c.478A>C	NP_001332811.1:p.Thr160Pro
NM_001345884.1:c.478A>C	NP_001332813.1:p.Thr160Pro
NM_001345885.1:c.478A>C	NP_001332814.1:p.Thr160Pro
NR_144301.1:n.799+740A>C
NR_144303.1:n.680+740A>C
NR_144305.1:n.665+740A>C
NR_144310.1:n.784+740A>C
XM_024454104.1:c.478A>C	XP_024309872.1:p.Thr160Pro
NM_017741.4:c.478A>C MANE Select	NP_060211.3:p.Thr160Pro
NM_001345880.2:c.478A>C	NP_001332809.1:p.Thr160Pro
NM_001345881.2:c.478A>C	NP_001332810.1:p.Thr160Pro
NM_001345882.2:c.478A>C	NP_001332811.1:p.Thr160Pro
NM_001345884.2:c.478A>C	NP_001332813.1:p.Thr160Pro
NM_001345885.2:c.478A>C	NP_001332814.1:p.Thr160Pro
NR_144301.2:n.798+740A>C
NR_144303.2:n.679+740A>C
NR_144305.2:n.664+740A>C
NR_144310.2:n.783+740A>C