Canonical Allele Identifier: CA2276046821

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540015_76540016delinsTA , CM000679.2:g.76540015_76540016delinsTA	GRCh38
NC_000017.10:g.74536097_74536098delinsTA , CM000679.1:g.74536097_74536098delinsTA	GRCh37
NC_000017.9:g.72047692_72047693delinsTA	NCBI36
NG_016702.1:g.17430_17431delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397633.7:n.46-490_46-489delinsTA (PRCD)
ENST00000465808.7:n.93-490_93-489delinsTA (PRCD)
ENST00000589145.1:c.-52-8325_-52-8324delinsTA (CYGB)	ENSP00000468559.1:n.-52-8325_-52-8324delinsTA
ENST00000590555.5:n.445-490_445-489delinsTA (PRCD)
ENST00000592432.5:n.249-490_249-489delinsTA (PRCD)
NR_033357.1:n.249-490_249-489delinsTA (PRCD)
XM_011524272.1:c.-52-8325_-52-8324delinsTA (CYGB)	XP_011522574.1:n.-52-8325_-52-8324delinsTA
XM_011525184.1:c.14-17_14-16delinsTA (PRCD)	XP_011523486.1:n.14-17_14-16delinsTA
XM_017024116.1:c.-52-8325_-52-8324delinsTA (CYGB)	XP_016879605.1:n.-52-8325_-52-8324delinsTA
XM_017025013.1:c.-127_-126delinsTA (PRCD)	XP_016880502.1:n.-127_-126delinsTA
XM_017025014.1:c.-127_-126delinsTA (PRCD)	XP_016880503.1:n.-127_-126delinsTA
XM_017025015.1:c.-127_-126delinsTA (PRCD)	XP_016880504.1:n.-127_-126delinsTA
NR_033357.2:n.249-490_249-489delinsTA (PRCD)