Canonical Allele Identifier: CA2276047128

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540523_76540533delinsTGGGGCAGCTA , CM000679.2:g.76540523_76540533delinsTGGGGCAGCTA	GRCh38
NC_000017.10:g.74536605_74536615delinsTGGGGCAGCTA , CM000679.1:g.74536605_74536615delinsTGGGGCAGCTA	GRCh37
NC_000017.9:g.72048200_72048210delinsTGGGGCAGCTA	NCBI36
NG_016702.1:g.17938_17948delinsTGGGGCAGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.93_103delinsTGGGGCAGCTA (PRCD) MANE Select	ENSP00000467661.1:p.Asp31=
ENST00000397630.7:n.53_63delinsTGGGGCAGCTA (PRCD)
ENST00000397633.7:n.64_74delinsTGGGGCAGCTA (PRCD)
ENST00000465808.7:n.111_121delinsTGGGGCAGCTA (PRCD)
ENST00000586148.1:c.93_103delinsTGGGGCAGCTA (PRCD)	ENSP00000465932.1:p.Asp31=
ENST00000589145.1:c.-52-8842_-52-8832delinsTAGCTGCCCCA (CYGB)	ENSP00000468559.1:n.-52-8842_-52-8832delinsTAGCTGCCCCA
ENST00000590555.5:n.463_473delinsTGGGGCAGCTA (PRCD)
ENST00000592014.5:c.93_103delinsTGGGGCAGCTA (PRCD)	ENSP00000467661.1:p.Asp31=
ENST00000592432.5:n.267_277delinsTGGGGCAGCTA (PRCD)
NM_001077620.2:c.93_103delinsTGGGGCAGCTA (PRCD)	NP_001071088.1:p.Asp31=
NR_033357.1:n.267_277delinsTGGGGCAGCTA (PRCD)
XM_011524272.1:c.-52-8842_-52-8832delinsTAGCTGCCCCA (CYGB)	XP_011522574.1:n.-52-8842_-52-8832delinsTAGCTGCCCCA
XM_011525184.1:c.216_226delinsTGGGGCAGCTA (PRCD)	XP_011523486.1:p.Asp72=
XM_017024116.1:c.-52-8842_-52-8832delinsTAGCTGCCCCA (CYGB)	XP_016879605.1:n.-52-8842_-52-8832delinsTAGCTGCCCCA
XM_017025013.1:c.93_103delinsTGGGGCAGCTA (PRCD)	XP_016880502.1:p.Asp31=
XM_017025014.1:c.93_103delinsTGGGGCAGCTA (PRCD)	XP_016880503.1:p.Asp31=
XM_017025015.1:c.93_103delinsTGGGGCAGCTA (PRCD)	XP_016880504.1:p.Asp31=
NM_001077620.3:c.93_103delinsTGGGGCAGCTA (PRCD) MANE Select	NP_001071088.1:p.Asp31=
NR_033357.2:n.267_277delinsTGGGGCAGCTA (PRCD)