Canonical Allele Identifier: CA2576440626

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540263_76540264insGGGCCC , CM000679.2:g.76540263_76540264insGGGCCC	GRCh38
NC_000017.10:g.74536345_74536346insGGGCCC , CM000679.1:g.74536345_74536346insGGGCCC	GRCh37
NC_000017.9:g.72047940_72047941insGGGCCC	NCBI36
NG_016702.1:g.17678_17679insGGGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.74+48_74+49insGGGCCC (PRCD) MANE Select	ENSP00000467661.1:n.74+48_74+49insGGGCCC
ENST00000397633.7:n.46-242_46-241insGGGCCC (PRCD)
ENST00000465808.7:n.93-242_93-241insGGGCCC (PRCD)
ENST00000586148.1:c.74+48_74+49insGGGCCC (PRCD)	ENSP00000465932.1:n.74+48_74+49insGGGCCC
ENST00000589145.1:c.-52-8573_-52-8572insGGGCCC (CYGB)	ENSP00000468559.1:n.-52-8573_-52-8572insGGGCCC
ENST00000590555.5:n.445-242_445-241insGGGCCC (PRCD)
ENST00000592014.5:c.74+48_74+49insGGGCCC (PRCD)	ENSP00000467661.1:n.74+48_74+49insGGGCCC
ENST00000592432.5:n.249-242_249-241insGGGCCC (PRCD)
NM_001077620.2:c.74+48_74+49insGGGCCC (PRCD)	NP_001071088.1:n.74+48_74+49insGGGCCC
NR_033357.1:n.249-242_249-241insGGGCCC (PRCD)
XM_011524272.1:c.-52-8573_-52-8572insGGGCCC (CYGB)	XP_011522574.1:n.-52-8573_-52-8572insGGGCCC
XM_011525184.1:c.197+48_197+49insGGGCCC (PRCD)	XP_011523486.1:n.197+48_197+49insGGGCCC
XM_017024116.1:c.-52-8573_-52-8572insGGGCCC (CYGB)	XP_016879605.1:n.-52-8573_-52-8572insGGGCCC
XM_017025013.1:c.74+48_74+49insGGGCCC (PRCD)	XP_016880502.1:n.74+48_74+49insGGGCCC
XM_017025014.1:c.74+48_74+49insGGGCCC (PRCD)	XP_016880503.1:n.74+48_74+49insGGGCCC
XM_017025015.1:c.74+48_74+49insGGGCCC (PRCD)	XP_016880504.1:n.74+48_74+49insGGGCCC
NM_001077620.3:c.74+48_74+49insGGGCCC (PRCD) MANE Select	NP_001071088.1:n.74+48_74+49insGGGCCC
NR_033357.2:n.249-242_249-241insGGGCCC (PRCD)