Canonical Allele Identifier: CA2640010065

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540257-G-GGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540259_76540260insCGG , CM000679.2:g.76540259_76540260insCGG	GRCh38
NC_000017.10:g.74536341_74536342insCGG , CM000679.1:g.74536341_74536342insCGG	GRCh37
NC_000017.9:g.72047936_72047937insCGG	NCBI36
NG_016702.1:g.17674_17675insCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.74+44_74+45insCGG (PRCD) MANE Select	ENSP00000467661.1:n.74+44_74+45insCGG
ENST00000397633.7:n.46-246_46-245insCGG (PRCD)
ENST00000465808.7:n.93-246_93-245insCGG (PRCD)
ENST00000586148.1:c.74+44_74+45insCGG (PRCD)	ENSP00000465932.1:n.74+44_74+45insCGG
ENST00000589145.1:c.-52-8567_-52-8566insGCC (CYGB)	ENSP00000468559.1:n.-52-8567_-52-8566insGCC
ENST00000590555.5:n.445-246_445-245insCGG (PRCD)
ENST00000592014.5:c.74+44_74+45insCGG (PRCD)	ENSP00000467661.1:n.74+44_74+45insCGG
ENST00000592432.5:n.249-246_249-245insCGG (PRCD)
NM_001077620.2:c.74+44_74+45insCGG (PRCD)	NP_001071088.1:n.74+44_74+45insCGG
NR_033357.1:n.249-246_249-245insCGG (PRCD)
XM_011524272.1:c.-52-8567_-52-8566insGCC (CYGB)	XP_011522574.1:n.-52-8567_-52-8566insGCC
XM_011525184.1:c.197+44_197+45insCGG (PRCD)	XP_011523486.1:n.197+44_197+45insCGG
XM_017024116.1:c.-52-8567_-52-8566insGCC (CYGB)	XP_016879605.1:n.-52-8567_-52-8566insGCC
XM_017025013.1:c.74+44_74+45insCGG (PRCD)	XP_016880502.1:n.74+44_74+45insCGG
XM_017025014.1:c.74+44_74+45insCGG (PRCD)	XP_016880503.1:n.74+44_74+45insCGG
XM_017025015.1:c.74+44_74+45insCGG (PRCD)	XP_016880504.1:n.74+44_74+45insCGG
NM_001077620.3:c.74+44_74+45insCGG (PRCD) MANE Select	NP_001071088.1:n.74+44_74+45insCGG
NR_033357.2:n.249-246_249-245insCGG (PRCD)