Canonical Allele Identifier: CA2640009373

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540073-G-GGGCCATTTTGGCCCCTCGCCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540078_76540100dup , CM000679.2:g.76540078_76540100dup	GRCh38
NC_000017.10:g.74536160_74536182dup , CM000679.1:g.74536160_74536182dup	GRCh37
NC_000017.9:g.72047755_72047777dup	NCBI36
NG_016702.1:g.17493_17515dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.-64_-42dup (PRCD) MANE Select	ENSP00000467661.1:n.-64_-42dup
ENST00000397633.7:n.46-427_46-405dup (PRCD)
ENST00000465808.7:n.93-427_93-405dup (PRCD)
ENST00000589145.1:c.-52-8405_-52-8383dup (CYGB)	ENSP00000468559.1:n.-52-8405_-52-8383dup
ENST00000590555.5:n.445-427_445-405dup (PRCD)
ENST00000592014.5:c.-64_-42dup (PRCD)	ENSP00000467661.1:n.-64_-42dup
ENST00000592432.5:n.249-427_249-405dup (PRCD)
NM_001077620.2:c.-64_-42dup (PRCD)	NP_001071088.1:n.-64_-42dup
NR_033357.1:n.249-427_249-405dup (PRCD)
XM_011524272.1:c.-52-8405_-52-8383dup (CYGB)	XP_011522574.1:n.-52-8405_-52-8383dup
XM_011525184.1:c.60_82dup (PRCD)	XP_011523486.1:p.Leu28HisfsTer?
XM_017024116.1:c.-52-8405_-52-8383dup (CYGB)	XP_016879605.1:n.-52-8405_-52-8383dup
XM_017025013.1:c.-64_-42dup (PRCD)	XP_016880502.1:n.-64_-42dup
XM_017025014.1:c.-64_-42dup (PRCD)	XP_016880503.1:n.-64_-42dup
XM_017025015.1:c.-64_-42dup (PRCD)	XP_016880504.1:n.-64_-42dup
NM_001077620.3:c.-64_-42dup (PRCD) MANE Select	NP_001071088.1:n.-64_-42dup
NR_033357.2:n.249-427_249-405dup (PRCD)