Canonical Allele Identifier: CA501890133

Gene: PRCD CYGB

Linked Data

• MyVariant Identifiers: chr17:g.74536235C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540153C>T , CM000679.2:g.76540153C>T	GRCh38
NC_000017.10:g.74536235C>T , CM000679.1:g.74536235C>T	GRCh37
NC_000017.9:g.72047830C>T	NCBI36
NG_016702.1:g.17568C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000592014.6:c.12C>T (PRCD) MANE Select	ENSP00000467661.1:p.Thr4=
ENST00000397633.7:n.46-352C>T (PRCD)
ENST00000465808.7:n.93-352C>T (PRCD)
ENST00000586148.1:c.12C>T (PRCD)	ENSP00000465932.1:p.Thr4=
ENST00000589145.1:c.-52-8462G>A (CYGB)	ENSP00000468559.1:n.-52-8462G>A
ENST00000590555.5:n.445-352C>T (PRCD)
ENST00000592014.5:c.12C>T (PRCD)	ENSP00000467661.1:p.Thr4=
ENST00000592432.5:n.249-352C>T (PRCD)
NM_001077620.2:c.12C>T (PRCD)	NP_001071088.1:p.Thr4=
NR_033357.1:n.249-352C>T (PRCD)
XM_011524272.1:c.-52-8462G>A (CYGB)	XP_011522574.1:n.-52-8462G>A
XM_011525184.1:c.135C>T (PRCD)	XP_011523486.1:p.Thr45=
XM_017024116.1:c.-52-8462G>A (CYGB)	XP_016879605.1:n.-52-8462G>A
XM_017025013.1:c.12C>T (PRCD)	XP_016880502.1:p.Thr4=
XM_017025014.1:c.12C>T (PRCD)	XP_016880503.1:p.Thr4=
XM_017025015.1:c.12C>T (PRCD)	XP_016880504.1:p.Thr4=
NM_001077620.3:c.12C>T (PRCD) MANE Select	NP_001071088.1:p.Thr4=
NR_033357.2:n.249-352C>T (PRCD)