Canonical Allele Identifier: CA627457877

Gene: PRCD CYGB

Linked Data

• dbSNP Id: rs1567910879
• gnomAD v2: 17-74536281-GCCAACCGAGT-G
• gnomAD v4: 17-76540199-GCCAACCGAGT-G
• MyVariant Identifiers: chr17:g.74536282_74536291del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540207_76540216del , CM000679.2:g.76540207_76540216del	GRCh38
NC_000017.10:g.74536289_74536298del , CM000679.1:g.74536289_74536298del	GRCh37
NC_000017.9:g.72047884_72047893del	NCBI36
NG_016702.1:g.17622_17631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.66_74+1del (PRCD)
ENST00000397633.7:n.46-298_46-289del (PRCD)
ENST00000465808.7:n.93-298_93-289del (PRCD)
ENST00000586148.1:c.66_74+1del (PRCD)
ENST00000589145.1:c.-52-8518_-52-8509del (CYGB)	ENSP00000468559.1:n.-52-8518_-52-8509del
ENST00000590555.5:n.445-298_445-289del (PRCD)
ENST00000592014.5:c.66_74+1del (PRCD)
ENST00000592432.5:n.249-298_249-289del (PRCD)
NM_001077620.2:c.66_74+1del (PRCD)
NR_033357.1:n.249-298_249-289del (PRCD)
XM_011524272.1:c.-52-8518_-52-8509del (CYGB)	XP_011522574.1:n.-52-8518_-52-8509del
XM_011525184.1:c.189_197+1del (PRCD)
XM_017024116.1:c.-52-8518_-52-8509del (CYGB)	XP_016879605.1:n.-52-8518_-52-8509del
XM_017025013.1:c.66_74+1del (PRCD)
XM_017025014.1:c.66_74+1del (PRCD)
XM_017025015.1:c.66_74+1del (PRCD)
NM_001077620.3:c.66_74+1del (PRCD)
NR_033357.2:n.249-298_249-289del (PRCD)