Canonical Allele Identifier: CA2640009635

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540249-GTCGGGGGGGGGGGGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540251_76540266del , CM000679.2:g.76540251_76540266del	GRCh38
NC_000017.10:g.74536333_74536348del , CM000679.1:g.74536333_74536348del	GRCh37
NC_000017.9:g.72047928_72047943del	NCBI36
NG_016702.1:g.17666_17681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.74+36_74+51del (PRCD) MANE Select	ENSP00000467661.1:n.74+36_74+51del
ENST00000397633.7:n.46-254_46-239del (PRCD)
ENST00000465808.7:n.93-254_93-239del (PRCD)
ENST00000586148.1:c.74+36_74+51del (PRCD)	ENSP00000465932.1:n.74+36_74+51del
ENST00000589145.1:c.-52-8574_-52-8559del (CYGB)	ENSP00000468559.1:n.-52-8574_-52-8559del
ENST00000590555.5:n.445-254_445-239del (PRCD)
ENST00000592014.5:c.74+36_74+51del (PRCD)	ENSP00000467661.1:n.74+36_74+51del
ENST00000592432.5:n.249-254_249-239del (PRCD)
NM_001077620.2:c.74+36_74+51del (PRCD)	NP_001071088.1:n.74+36_74+51del
NR_033357.1:n.249-254_249-239del (PRCD)
XM_011524272.1:c.-52-8574_-52-8559del (CYGB)	XP_011522574.1:n.-52-8574_-52-8559del
XM_011525184.1:c.197+36_197+51del (PRCD)	XP_011523486.1:n.197+36_197+51del
XM_017024116.1:c.-52-8574_-52-8559del (CYGB)	XP_016879605.1:n.-52-8574_-52-8559del
XM_017025013.1:c.74+36_74+51del (PRCD)	XP_016880502.1:n.74+36_74+51del
XM_017025014.1:c.74+36_74+51del (PRCD)	XP_016880503.1:n.74+36_74+51del
XM_017025015.1:c.74+36_74+51del (PRCD)	XP_016880504.1:n.74+36_74+51del
NM_001077620.3:c.74+36_74+51del (PRCD) MANE Select	NP_001071088.1:n.74+36_74+51del
NR_033357.2:n.249-254_249-239del (PRCD)