Canonical Allele Identifier: CA986412620

Gene: PRCD CYGB

Linked Data

• dbSNP Id: rs2074974709
• gnomAD v3: 17-76540266-T-TGGGGGGGGGGGGGGGG
• gnomAD v4: 17-76540266-T-TGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540270_76540271insGGGGGGGGGGGGGGGG , CM000679.2:g.76540270_76540271insGGGGGGGGGGGGGGGG	GRCh38
NC_000017.10:g.74536352_74536353insGGGGGGGGGGGGGGGG , CM000679.1:g.74536352_74536353insGGGGGGGGGGGGGGGG	GRCh37
NC_000017.9:g.72047947_72047948insGGGGGGGGGGGGGGGG	NCBI36
NG_016702.1:g.17685_17686insGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.74+55_74+56insGGGGGGGGGGGGGGGG (PRCD) MANE Select	ENSP00000467661.1:n.74+55_74+56insGGGGGGGGGGGGGGGG
ENST00000397633.7:n.46-235_46-234insGGGGGGGGGGGGGGGG (PRCD)
ENST00000465808.7:n.93-235_93-234insGGGGGGGGGGGGGGGG (PRCD)
ENST00000586148.1:c.74+55_74+56insGGGGGGGGGGGGGGGG (PRCD)	ENSP00000465932.1:n.74+55_74+56insGGGGGGGGGGGGGGGG
ENST00000589145.1:c.-52-8576_-52-8575insCCCCCCCCCCCCCCCC (CYGB)	ENSP00000468559.1:n.-52-8576_-52-8575insCCCCCCCCCCCCCCCC
ENST00000590555.5:n.445-235_445-234insGGGGGGGGGGGGGGGG (PRCD)
ENST00000592014.5:c.74+55_74+56insGGGGGGGGGGGGGGGG (PRCD)	ENSP00000467661.1:n.74+55_74+56insGGGGGGGGGGGGGGGG
ENST00000592432.5:n.249-235_249-234insGGGGGGGGGGGGGGGG (PRCD)
NM_001077620.2:c.74+55_74+56insGGGGGGGGGGGGGGGG (PRCD)	NP_001071088.1:n.74+55_74+56insGGGGGGGGGGGGGGGG
NR_033357.1:n.249-235_249-234insGGGGGGGGGGGGGGGG (PRCD)
XM_011524272.1:c.-52-8576_-52-8575insCCCCCCCCCCCCCCCC (CYGB)	XP_011522574.1:n.-52-8576_-52-8575insCCCCCCCCCCCCCCCC
XM_011525184.1:c.197+55_197+56insGGGGGGGGGGGGGGGG (PRCD)	XP_011523486.1:n.197+55_197+56insGGGGGGGGGGGGGGGG
XM_017024116.1:c.-52-8576_-52-8575insCCCCCCCCCCCCCCCC (CYGB)	XP_016879605.1:n.-52-8576_-52-8575insCCCCCCCCCCCCCCCC
XM_017025013.1:c.74+55_74+56insGGGGGGGGGGGGGGGG (PRCD)	XP_016880502.1:n.74+55_74+56insGGGGGGGGGGGGGGGG
XM_017025014.1:c.74+55_74+56insGGGGGGGGGGGGGGGG (PRCD)	XP_016880503.1:n.74+55_74+56insGGGGGGGGGGGGGGGG
XM_017025015.1:c.74+55_74+56insGGGGGGGGGGGGGGGG (PRCD)	XP_016880504.1:n.74+55_74+56insGGGGGGGGGGGGGGGG
NM_001077620.3:c.74+55_74+56insGGGGGGGGGGGGGGGG (PRCD) MANE Select	NP_001071088.1:n.74+55_74+56insGGGGGGGGGGGGGGGG
NR_033357.2:n.249-235_249-234insGGGGGGGGGGGGGGGG (PRCD)