Canonical Allele Identifier: CA2640009385

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540088-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540089del , CM000679.2:g.76540089del	GRCh38
NC_000017.10:g.74536171del , CM000679.1:g.74536171del	GRCh37
NC_000017.9:g.72047766del	NCBI36
NG_016702.1:g.17504del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.-53del (PRCD) MANE Select	ENSP00000467661.1:n.-53del
ENST00000397633.7:n.46-416del (PRCD)
ENST00000465808.7:n.93-416del (PRCD)
ENST00000589145.1:c.-52-8398del (CYGB)	ENSP00000468559.1:n.-52-8398del
ENST00000590555.5:n.445-416del (PRCD)
ENST00000592014.5:c.-53del (PRCD)	ENSP00000467661.1:n.-53del
ENST00000592432.5:n.249-416del (PRCD)
NM_001077620.2:c.-53del (PRCD)	NP_001071088.1:n.-53del
NR_033357.1:n.249-416del (PRCD)
XM_011524272.1:c.-52-8398del (CYGB)	XP_011522574.1:n.-52-8398del
XM_011525184.1:c.71del (PRCD)	XP_011523486.1:p.Leu24ProfsTer?
XM_017024116.1:c.-52-8398del (CYGB)	XP_016879605.1:n.-52-8398del
XM_017025013.1:c.-53del (PRCD)	XP_016880502.1:n.-53del
XM_017025014.1:c.-53del (PRCD)	XP_016880503.1:n.-53del
XM_017025015.1:c.-53del (PRCD)	XP_016880504.1:n.-53del
NM_001077620.3:c.-53del (PRCD) MANE Select	NP_001071088.1:n.-53del
NR_033357.2:n.249-416del (PRCD)