Canonical Allele Identifier: CA2276046838

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540050_76540051delinsCA , CM000679.2:g.76540050_76540051delinsCA	GRCh38
NC_000017.10:g.74536132_74536133delinsCA , CM000679.1:g.74536132_74536133delinsCA	GRCh37
NC_000017.9:g.72047727_72047728delinsCA	NCBI36
NG_016702.1:g.17465_17466delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.-92_-91delinsCA (PRCD) MANE Select	ENSP00000467661.1:n.-92_-91delinsCA
ENST00000397633.7:n.46-455_46-454delinsCA (PRCD)
ENST00000465808.7:n.93-455_93-454delinsCA (PRCD)
ENST00000589145.1:c.-52-8360_-52-8359delinsTG (CYGB)	ENSP00000468559.1:n.-52-8360_-52-8359delinsTG
ENST00000590555.5:n.445-455_445-454delinsCA (PRCD)
ENST00000592014.5:c.-92_-91delinsCA (PRCD)	ENSP00000467661.1:n.-92_-91delinsCA
ENST00000592432.5:n.249-455_249-454delinsCA (PRCD)
NM_001077620.2:c.-92_-91delinsCA (PRCD)	NP_001071088.1:n.-92_-91delinsCA
NR_033357.1:n.249-455_249-454delinsCA (PRCD)
XM_011524272.1:c.-52-8360_-52-8359delinsTG (CYGB)	XP_011522574.1:n.-52-8360_-52-8359delinsTG
XM_011525184.1:c.32_33delinsCA (PRCD)	XP_011523486.1:p.Ala11=
XM_017024116.1:c.-52-8360_-52-8359delinsTG (CYGB)	XP_016879605.1:n.-52-8360_-52-8359delinsTG
XM_017025013.1:c.-92_-91delinsCA (PRCD)	XP_016880502.1:n.-92_-91delinsCA
XM_017025014.1:c.-92_-91delinsCA (PRCD)	XP_016880503.1:n.-92_-91delinsCA
XM_017025015.1:c.-92_-91delinsCA (PRCD)	XP_016880504.1:n.-92_-91delinsCA
NM_001077620.3:c.-92_-91delinsCA (PRCD) MANE Select	NP_001071088.1:n.-92_-91delinsCA
NR_033357.2:n.249-455_249-454delinsCA (PRCD)