Canonical Allele Identifier: CA2640010481

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540265-A-AGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540265_76540266insGGGGGGGGGG , CM000679.2:g.76540265_76540266insGGGGGGGGGG	GRCh38
NC_000017.10:g.74536347_74536348insGGGGGGGGGG , CM000679.1:g.74536347_74536348insGGGGGGGGGG	GRCh37
NC_000017.9:g.72047942_72047943insGGGGGGGGGG	NCBI36
NG_016702.1:g.17680_17681insGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.74+50_74+51insGGGGGGGGGG (PRCD) MANE Select	ENSP00000467661.1:n.74+50_74+51insGGGGGGGGGG
ENST00000397633.7:n.46-240_46-239insGGGGGGGGGG (PRCD)
ENST00000465808.7:n.93-240_93-239insGGGGGGGGGG (PRCD)
ENST00000586148.1:c.74+50_74+51insGGGGGGGGGG (PRCD)	ENSP00000465932.1:n.74+50_74+51insGGGGGGGGGG
ENST00000589145.1:c.-52-8575_-52-8574insCCCCCCCCCC (CYGB)	ENSP00000468559.1:n.-52-8575_-52-8574insCCCCCCCCCC
ENST00000590555.5:n.445-240_445-239insGGGGGGGGGG (PRCD)
ENST00000592014.5:c.74+50_74+51insGGGGGGGGGG (PRCD)	ENSP00000467661.1:n.74+50_74+51insGGGGGGGGGG
ENST00000592432.5:n.249-240_249-239insGGGGGGGGGG (PRCD)
NM_001077620.2:c.74+50_74+51insGGGGGGGGGG (PRCD)	NP_001071088.1:n.74+50_74+51insGGGGGGGGGG
NR_033357.1:n.249-240_249-239insGGGGGGGGGG (PRCD)
XM_011524272.1:c.-52-8575_-52-8574insCCCCCCCCCC (CYGB)	XP_011522574.1:n.-52-8575_-52-8574insCCCCCCCCCC
XM_011525184.1:c.197+50_197+51insGGGGGGGGGG (PRCD)	XP_011523486.1:n.197+50_197+51insGGGGGGGGGG
XM_017024116.1:c.-52-8575_-52-8574insCCCCCCCCCC (CYGB)	XP_016879605.1:n.-52-8575_-52-8574insCCCCCCCCCC
XM_017025013.1:c.74+50_74+51insGGGGGGGGGG (PRCD)	XP_016880502.1:n.74+50_74+51insGGGGGGGGGG
XM_017025014.1:c.74+50_74+51insGGGGGGGGGG (PRCD)	XP_016880503.1:n.74+50_74+51insGGGGGGGGGG
XM_017025015.1:c.74+50_74+51insGGGGGGGGGG (PRCD)	XP_016880504.1:n.74+50_74+51insGGGGGGGGGG
NM_001077620.3:c.74+50_74+51insGGGGGGGGGG (PRCD) MANE Select	NP_001071088.1:n.74+50_74+51insGGGGGGGGGG
NR_033357.2:n.249-240_249-239insGGGGGGGGGG (PRCD)