Canonical Allele Identifier: CA2520577018

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540272-T-TGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540275_76540276insGGGGGGG , CM000679.2:g.76540275_76540276insGGGGGGG	GRCh38
NC_000017.10:g.74536357_74536358insGGGGGGG , CM000679.1:g.74536357_74536358insGGGGGGG	GRCh37
NC_000017.9:g.72047952_72047953insGGGGGGG	NCBI36
NG_016702.1:g.17690_17691insGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.74+60_74+61insGGGGGGG (PRCD) MANE Select	ENSP00000467661.1:n.74+60_74+61insGGGGGGG
ENST00000397633.7:n.46-230_46-229insGGGGGGG (PRCD)
ENST00000465808.7:n.93-230_93-229insGGGGGGG (PRCD)
ENST00000586148.1:c.74+60_74+61insGGGGGGG (PRCD)	ENSP00000465932.1:n.74+60_74+61insGGGGGGG
ENST00000589145.1:c.-52-8582_-52-8581insCCCCCCC (CYGB)	ENSP00000468559.1:n.-52-8582_-52-8581insCCCCCCC
ENST00000590555.5:n.445-230_445-229insGGGGGGG (PRCD)
ENST00000592014.5:c.74+60_74+61insGGGGGGG (PRCD)	ENSP00000467661.1:n.74+60_74+61insGGGGGGG
ENST00000592432.5:n.249-230_249-229insGGGGGGG (PRCD)
NM_001077620.2:c.74+60_74+61insGGGGGGG (PRCD)	NP_001071088.1:n.74+60_74+61insGGGGGGG
NR_033357.1:n.249-230_249-229insGGGGGGG (PRCD)
XM_011524272.1:c.-52-8582_-52-8581insCCCCCCC (CYGB)	XP_011522574.1:n.-52-8582_-52-8581insCCCCCCC
XM_011525184.1:c.197+60_197+61insGGGGGGG (PRCD)	XP_011523486.1:n.197+60_197+61insGGGGGGG
XM_017024116.1:c.-52-8582_-52-8581insCCCCCCC (CYGB)	XP_016879605.1:n.-52-8582_-52-8581insCCCCCCC
XM_017025013.1:c.74+60_74+61insGGGGGGG (PRCD)	XP_016880502.1:n.74+60_74+61insGGGGGGG
XM_017025014.1:c.74+60_74+61insGGGGGGG (PRCD)	XP_016880503.1:n.74+60_74+61insGGGGGGG
XM_017025015.1:c.74+60_74+61insGGGGGGG (PRCD)	XP_016880504.1:n.74+60_74+61insGGGGGGG
NM_001077620.3:c.74+60_74+61insGGGGGGG (PRCD) MANE Select	NP_001071088.1:n.74+60_74+61insGGGGGGG
NR_033357.2:n.249-230_249-229insGGGGGGG (PRCD)