Canonical Allele Identifier: CA2640011608

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540523-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540527del , CM000679.2:g.76540527del	GRCh38
NC_000017.10:g.74536609del , CM000679.1:g.74536609del	GRCh37
NC_000017.9:g.72048204del	NCBI36
NG_016702.1:g.17942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.97del (PRCD) MANE Select	ENSP00000467661.1:p.Ala33GlnfsTer21
ENST00000397630.7:n.57del (PRCD)
ENST00000397633.7:n.68del (PRCD)
ENST00000465808.7:n.115del (PRCD)
ENST00000586148.1:c.97del (PRCD)	ENSP00000465932.1:p.Ala33GlnfsTer21
ENST00000589145.1:c.-52-8833del (CYGB)	ENSP00000468559.1:n.-52-8833del
ENST00000590555.5:n.467del (PRCD)
ENST00000592014.5:c.97del (PRCD)	ENSP00000467661.1:p.Ala33GlnfsTer21
ENST00000592432.5:n.271del (PRCD)
NM_001077620.2:c.97del (PRCD)	NP_001071088.1:p.Ala33GlnfsTer21
NR_033357.1:n.271del (PRCD)
XM_011524272.1:c.-52-8833del (CYGB)	XP_011522574.1:n.-52-8833del
XM_011525184.1:c.220del (PRCD)	XP_011523486.1:p.Ala74GlnfsTer21
XM_017024116.1:c.-52-8833del (CYGB)	XP_016879605.1:n.-52-8833del
XM_017025013.1:c.97del (PRCD)	XP_016880502.1:p.Ala33GlnfsTer21
XM_017025014.1:c.97del (PRCD)	XP_016880503.1:p.Ala33GlnfsTer21
XM_017025015.1:c.97del (PRCD)	XP_016880504.1:p.Ala33GlnfsTer21
NM_001077620.3:c.97del (PRCD) MANE Select	NP_001071088.1:p.Ala33GlnfsTer21
NR_033357.2:n.271del (PRCD)