Canonical Allele Identifier: CA2276046782

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76539941G= , CM000679.2:g.76539941G=	GRCh38
NC_000017.10:g.74536023G= , CM000679.1:g.74536023G=	GRCh37
NC_000017.9:g.72047618G=	NCBI36
NG_016702.1:g.17356G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397633.7:n.46-564G= (PRCD)
ENST00000465808.7:n.93-564G= (PRCD)
ENST00000589145.1:c.-52-8250C= (CYGB)	ENSP00000468559.1:n.-52-8250C=
ENST00000590555.5:n.445-564G= (PRCD)
ENST00000592432.5:n.249-564G= (PRCD)
NR_033357.1:n.249-564G= (PRCD)
XM_011524272.1:c.-52-8250C= (CYGB)	XP_011522574.1:n.-52-8250C=
XM_011525184.1:c.14-91G= (PRCD)	XP_011523486.1:n.14-91G=
XM_017024116.1:c.-52-8250C= (CYGB)	XP_016879605.1:n.-52-8250C=
XM_017025013.1:c.-201G= (PRCD)	XP_016880502.1:n.-201G=
XM_017025014.1:c.-201G= (PRCD)	XP_016880503.1:n.-201G=
XM_017025015.1:c.-201G= (PRCD)	XP_016880504.1:n.-201G=
NR_033357.2:n.249-564G= (PRCD)