Canonical Allele Identifier: CA2276046796

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76539964T= , CM000679.2:g.76539964T=	GRCh38
NC_000017.10:g.74536046T= , CM000679.1:g.74536046T=	GRCh37
NC_000017.9:g.72047641T=	NCBI36
NG_016702.1:g.17379T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397633.7:n.46-541T= (PRCD)
ENST00000465808.7:n.93-541T= (PRCD)
ENST00000589145.1:c.-52-8273A= (CYGB)	ENSP00000468559.1:n.-52-8273A=
ENST00000590555.5:n.445-541T= (PRCD)
ENST00000592432.5:n.249-541T= (PRCD)
NR_033357.1:n.249-541T= (PRCD)
XM_011524272.1:c.-52-8273A= (CYGB)	XP_011522574.1:n.-52-8273A=
XM_011525184.1:c.14-68T= (PRCD)	XP_011523486.1:n.14-68T=
XM_017024116.1:c.-52-8273A= (CYGB)	XP_016879605.1:n.-52-8273A=
XM_017025013.1:c.-178T= (PRCD)	XP_016880502.1:n.-178T=
XM_017025014.1:c.-178T= (PRCD)	XP_016880503.1:n.-178T=
XM_017025015.1:c.-178T= (PRCD)	XP_016880504.1:n.-178T=
NR_033357.2:n.249-541T= (PRCD)