Canonical Allele Identifier: CA2276047106

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540483_76540484delinsTC , CM000679.2:g.76540483_76540484delinsTC	GRCh38
NC_000017.10:g.74536565_74536566delinsTC , CM000679.1:g.74536565_74536566delinsTC	GRCh37
NC_000017.9:g.72048160_72048161delinsTC	NCBI36
NG_016702.1:g.17898_17899delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.75-22_75-21delinsTC (PRCD) MANE Select	ENSP00000467661.1:n.75-22_75-21delinsTC
ENST00000397630.7:n.13_14delinsTC (PRCD)
ENST00000397633.7:n.46-22_46-21delinsTC (PRCD)
ENST00000465808.7:n.93-22_93-21delinsTC (PRCD)
ENST00000586148.1:c.75-22_75-21delinsTC (PRCD)	ENSP00000465932.1:n.75-22_75-21delinsTC
ENST00000589145.1:c.-52-8793_-52-8792delinsGA (CYGB)	ENSP00000468559.1:n.-52-8793_-52-8792delinsGA
ENST00000590555.5:n.445-22_445-21delinsTC (PRCD)
ENST00000592014.5:c.75-22_75-21delinsTC (PRCD)	ENSP00000467661.1:n.75-22_75-21delinsTC
ENST00000592432.5:n.249-22_249-21delinsTC (PRCD)
NM_001077620.2:c.75-22_75-21delinsTC (PRCD)	NP_001071088.1:n.75-22_75-21delinsTC
NR_033357.1:n.249-22_249-21delinsTC (PRCD)
XM_011524272.1:c.-52-8793_-52-8792delinsGA (CYGB)	XP_011522574.1:n.-52-8793_-52-8792delinsGA
XM_011525184.1:c.198-22_198-21delinsTC (PRCD)	XP_011523486.1:n.198-22_198-21delinsTC
XM_017024116.1:c.-52-8793_-52-8792delinsGA (CYGB)	XP_016879605.1:n.-52-8793_-52-8792delinsGA
XM_017025013.1:c.75-22_75-21delinsTC (PRCD)	XP_016880502.1:n.75-22_75-21delinsTC
XM_017025014.1:c.75-22_75-21delinsTC (PRCD)	XP_016880503.1:n.75-22_75-21delinsTC
XM_017025015.1:c.75-22_75-21delinsTC (PRCD)	XP_016880504.1:n.75-22_75-21delinsTC
NM_001077620.3:c.75-22_75-21delinsTC (PRCD) MANE Select	NP_001071088.1:n.75-22_75-21delinsTC
NR_033357.2:n.249-22_249-21delinsTC (PRCD)