Canonical Allele Identifier: CA2640009360

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540060-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540064_76540065del , CM000679.2:g.76540064_76540065del	GRCh38
NC_000017.10:g.74536146_74536147del , CM000679.1:g.74536146_74536147del	GRCh37
NC_000017.9:g.72047741_72047742del	NCBI36
NG_016702.1:g.17479_17480del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.-78_-77del (PRCD) MANE Select	ENSP00000467661.1:n.-78_-77del
ENST00000397633.7:n.46-441_46-440del (PRCD)
ENST00000465808.7:n.93-441_93-440del (PRCD)
ENST00000589145.1:c.-52-8371_-52-8370del (CYGB)	ENSP00000468559.1:n.-52-8371_-52-8370del
ENST00000590555.5:n.445-441_445-440del (PRCD)
ENST00000592014.5:c.-78_-77del (PRCD)	ENSP00000467661.1:n.-78_-77del
ENST00000592432.5:n.249-441_249-440del (PRCD)
NM_001077620.2:c.-78_-77del (PRCD)	NP_001071088.1:n.-78_-77del
NR_033357.1:n.249-441_249-440del (PRCD)
XM_011524272.1:c.-52-8371_-52-8370del (CYGB)	XP_011522574.1:n.-52-8371_-52-8370del
XM_011525184.1:c.46_47del (PRCD)	XP_011523486.1:p.Ser16LeufsTer?
XM_017024116.1:c.-52-8371_-52-8370del (CYGB)	XP_016879605.1:n.-52-8371_-52-8370del
XM_017025013.1:c.-78_-77del (PRCD)	XP_016880502.1:n.-78_-77del
XM_017025014.1:c.-78_-77del (PRCD)	XP_016880503.1:n.-78_-77del
XM_017025015.1:c.-78_-77del (PRCD)	XP_016880504.1:n.-78_-77del
NM_001077620.3:c.-78_-77del (PRCD) MANE Select	NP_001071088.1:n.-78_-77del
NR_033357.2:n.249-441_249-440del (PRCD)