Canonical Allele Identifier: CA2276047129

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540525G= , CM000679.2:g.76540525G=	GRCh38
NC_000017.10:g.74536607G= , CM000679.1:g.74536607G=	GRCh37
NC_000017.9:g.72048202G=	NCBI36
NG_016702.1:g.17940G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.95G= (PRCD) MANE Select	ENSP00000467661.1:p.Gly32=
ENST00000397630.7:n.55G= (PRCD)
ENST00000397633.7:n.66G= (PRCD)
ENST00000465808.7:n.113G= (PRCD)
ENST00000586148.1:c.95G= (PRCD)	ENSP00000465932.1:p.Gly32=
ENST00000589145.1:c.-52-8834C= (CYGB)	ENSP00000468559.1:n.-52-8834C=
ENST00000590555.5:n.465G= (PRCD)
ENST00000592014.5:c.95G= (PRCD)	ENSP00000467661.1:p.Gly32=
ENST00000592432.5:n.269G= (PRCD)
NM_001077620.2:c.95G= (PRCD)	NP_001071088.1:p.Gly32=
NR_033357.1:n.269G= (PRCD)
XM_011524272.1:c.-52-8834C= (CYGB)	XP_011522574.1:n.-52-8834C=
XM_011525184.1:c.218G= (PRCD)	XP_011523486.1:p.Gly73=
XM_017024116.1:c.-52-8834C= (CYGB)	XP_016879605.1:n.-52-8834C=
XM_017025013.1:c.95G= (PRCD)	XP_016880502.1:p.Gly32=
XM_017025014.1:c.95G= (PRCD)	XP_016880503.1:p.Gly32=
XM_017025015.1:c.95G= (PRCD)	XP_016880504.1:p.Gly32=
NM_001077620.3:c.95G= (PRCD) MANE Select	NP_001071088.1:p.Gly32=
NR_033357.2:n.269G= (PRCD)