Canonical Allele Identifier: CA2810474653

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540191_76540194del , CM000679.2:g.76540191_76540194del	GRCh38
NC_000017.10:g.74536273_74536276del , CM000679.1:g.74536273_74536276del	GRCh37
NC_000017.9:g.72047868_72047871del	NCBI36
NG_016702.1:g.17606_17609del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.50_53del (PRCD) MANE Select	ENSP00000467661.1:p.Arg17HisfsTer?
ENST00000397633.7:n.46-314_46-311del (PRCD)
ENST00000465808.7:n.93-314_93-311del (PRCD)
ENST00000586148.1:c.50_53del (PRCD)	ENSP00000465932.1:p.Arg17HisfsTer?
ENST00000589145.1:c.-52-8503_-52-8500del (CYGB)	ENSP00000468559.1:n.-52-8503_-52-8500del
ENST00000590555.5:n.445-314_445-311del (PRCD)
ENST00000592014.5:c.50_53del (PRCD)	ENSP00000467661.1:p.Arg17HisfsTer?
ENST00000592432.5:n.249-314_249-311del (PRCD)
NM_001077620.2:c.50_53del (PRCD)	NP_001071088.1:p.Arg17HisfsTer?
NR_033357.1:n.249-314_249-311del (PRCD)
XM_011524272.1:c.-52-8503_-52-8500del (CYGB)	XP_011522574.1:n.-52-8503_-52-8500del
XM_011525184.1:c.173_176del (PRCD)	XP_011523486.1:p.Arg58HisfsTer?
XM_017024116.1:c.-52-8503_-52-8500del (CYGB)	XP_016879605.1:n.-52-8503_-52-8500del
XM_017025013.1:c.50_53del (PRCD)	XP_016880502.1:p.Arg17HisfsTer?
XM_017025014.1:c.50_53del (PRCD)	XP_016880503.1:p.Arg17HisfsTer?
XM_017025015.1:c.50_53del (PRCD)	XP_016880504.1:p.Arg17HisfsTer?
NM_001077620.3:c.50_53del (PRCD) MANE Select	NP_001071088.1:p.Arg17HisfsTer?
NR_033357.2:n.249-314_249-311del (PRCD)