Canonical Allele Identifier: CA9971859
Community Standard Title: NM_012469.4(PRPF6):c.282C>T (p.Tyr94=)
Gene: PRPF6 HGNC NCBI
ZNF512B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63984948C>T , CM000682.2:g.63984948C>T GRCh38
NC_000020.10:g.62616301C>T , CM000682.1:g.62616301C>T GRCh37
NC_000020.9:g.62086745C>T NCBI36
NG_029719.1:g.8871C>T

Transcript Alleles

HGVS Amino-acid Change
NM_012469.4:c.282C>T (PRPF6) MANE Select NP_036601.2:p.Tyr94=
ENST00000266079.5:c.282C>T (PRPF6) MANE Select ENSP00000266079.4:p.Tyr94=
NM_012469.3:c.282C>T (PRPF6) NP_036601.2:p.Tyr94=
ENST00000217130.4:c.-6-16992G>A (ZNF512B) ENSP00000217130.3:n.-6-16992G>A
ENST00000266079.4:c.282C>T (PRPF6) ENSP00000266079.4:p.Tyr94=
ENST00000450537.5:c.-5-16993G>A (ZNF512B) ENSP00000393795.1:n.-5-16993G>A
XM_006723769.2:c.282C>T (PRPF6) XP_006723832.1:p.Tyr94=
XM_006723769.3:c.282C>T (PRPF6) XP_006723832.1:p.Tyr94=