Canonical Allele Identifier: CA2640009140

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76539918-CTTGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76539919_76539922del , CM000679.2:g.76539919_76539922del	GRCh38
NC_000017.10:g.74536001_74536004del , CM000679.1:g.74536001_74536004del	GRCh37
NC_000017.9:g.72047596_72047599del	NCBI36
NG_016702.1:g.17334_17337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397633.7:n.46-586_46-583del (PRCD)
ENST00000465808.7:n.93-586_93-583del (PRCD)
ENST00000589145.1:c.-52-8231_-52-8228del (CYGB)	ENSP00000468559.1:n.-52-8231_-52-8228del
ENST00000590555.5:n.445-586_445-583del (PRCD)
ENST00000592432.5:n.249-586_249-583del (PRCD)
NR_033357.1:n.249-586_249-583del (PRCD)
XM_011524272.1:c.-52-8231_-52-8228del (CYGB)	XP_011522574.1:n.-52-8231_-52-8228del
XM_011525184.1:c.14-113_14-110del (PRCD)	XP_011523486.1:n.14-113_14-110del
XM_017024116.1:c.-52-8231_-52-8228del (CYGB)	XP_016879605.1:n.-52-8231_-52-8228del
XM_017025013.1:c.-223_-220del (PRCD)	XP_016880502.1:n.-223_-220del
XM_017025014.1:c.-223_-220del (PRCD)	XP_016880503.1:n.-223_-220del
XM_017025015.1:c.-223_-220del (PRCD)	XP_016880504.1:n.-223_-220del
NR_033357.2:n.249-586_249-583del (PRCD)