Canonical Allele Identifier: CA775195867

Gene: PRCD CYGB

Linked Data

• dbSNP Id: rs1302638752
• gnomAD v3: 17-76540071-TG-T
• gnomAD v4: 17-76540071-TG-T
• MyVariant Identifiers: chr17:g.74536154del (hg19) ; chr17:g.76540072del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540075del , CM000679.2:g.76540075del	GRCh38
NC_000017.10:g.74536157del , CM000679.1:g.74536157del	GRCh37
NC_000017.9:g.72047752del	NCBI36
NG_016702.1:g.17490del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.-67del (PRCD) MANE Select	ENSP00000467661.1:n.-67del
ENST00000397633.7:n.46-430del (PRCD)
ENST00000465808.7:n.93-430del (PRCD)
ENST00000589145.1:c.-52-8381del (CYGB)	ENSP00000468559.1:n.-52-8381del
ENST00000590555.5:n.445-430del (PRCD)
ENST00000592014.5:c.-67del (PRCD)	ENSP00000467661.1:n.-67del
ENST00000592432.5:n.249-430del (PRCD)
NM_001077620.2:c.-67del (PRCD)	NP_001071088.1:n.-67del
NR_033357.1:n.249-430del (PRCD)
XM_011524272.1:c.-52-8381del (CYGB)	XP_011522574.1:n.-52-8381del
XM_011525184.1:c.57del (PRCD)	XP_011523486.1:p.Pro20HisfsTer?
XM_017024116.1:c.-52-8381del (CYGB)	XP_016879605.1:n.-52-8381del
XM_017025013.1:c.-67del (PRCD)	XP_016880502.1:n.-67del
XM_017025014.1:c.-67del (PRCD)	XP_016880503.1:n.-67del
XM_017025015.1:c.-67del (PRCD)	XP_016880504.1:n.-67del
NM_001077620.3:c.-67del (PRCD) MANE Select	NP_001071088.1:n.-67del
NR_033357.2:n.249-430del (PRCD)