Canonical Allele Identifier: CA2810474831

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540264_76540265insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA , CM000679.2:g.76540264_76540265insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA	GRCh38
NC_000017.10:g.74536346_74536347insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA , CM000679.1:g.74536346_74536347insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA	GRCh37
NC_000017.9:g.72047941_72047942insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA	NCBI36
NG_016702.1:g.17679_17680insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD) MANE Select	ENSP00000467661.1:n.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGG...
ENST00000397633.7:n.46-241_46-240insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)
ENST00000465808.7:n.93-241_93-240insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)
ENST00000586148.1:c.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)	ENSP00000465932.1:n.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGG...
ENST00000589145.1:c.-52-8574_-52-8573insTTCCCCCCCCCCCCCCCCCCCCCCCCCCTTGGG (CYGB)	ENSP00000468559.1:n.-52-8574_-52-8573insTTCCCCCCCCCCCCCCCCCCC...
ENST00000590555.5:n.445-241_445-240insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)
ENST00000592014.5:c.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)	ENSP00000467661.1:n.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGG...
ENST00000592432.5:n.249-241_249-240insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)
NM_001077620.2:c.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)	NP_001071088.1:n.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGG...
NR_033357.1:n.249-241_249-240insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)
XM_011524272.1:c.-52-8574_-52-8573insTTCCCCCCCCCCCCCCCCCCCCCCCCCCTTGGG (CYGB)	XP_011522574.1:n.-52-8574_-52-8573insTTCCCCCCCCCCCCCCCCCCCCCC...
XM_011525184.1:c.197+49_197+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)	XP_011523486.1:n.197+49_197+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGG...
XM_017024116.1:c.-52-8574_-52-8573insTTCCCCCCCCCCCCCCCCCCCCCCCCCCTTGGG (CYGB)	XP_016879605.1:n.-52-8574_-52-8573insTTCCCCCCCCCCCCCCCCCCCCCC...
XM_017025013.1:c.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)	XP_016880502.1:n.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_017025014.1:c.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)	XP_016880503.1:n.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_017025015.1:c.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)	XP_016880504.1:n.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001077620.3:c.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD) MANE Select	NP_001071088.1:n.74+49_74+50insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGG...
NR_033357.2:n.249-241_249-240insCCCAAGGGGGGGGGGGGGGGGGGGGGGGGGGAA (PRCD)