Canonical Allele Identifier: CA2276047043

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540371_76540372delinsCA , CM000679.2:g.76540371_76540372delinsCA	GRCh38
NC_000017.10:g.74536453_74536454delinsCA , CM000679.1:g.74536453_74536454delinsCA	GRCh37
NC_000017.9:g.72048048_72048049delinsCA	NCBI36
NG_016702.1:g.17786_17787delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.75-134_75-133delinsCA (PRCD) MANE Select	ENSP00000467661.1:n.75-134_75-133delinsCA
ENST00000397633.7:n.46-134_46-133delinsCA (PRCD)
ENST00000465808.7:n.93-134_93-133delinsCA (PRCD)
ENST00000586148.1:c.75-134_75-133delinsCA (PRCD)	ENSP00000465932.1:n.75-134_75-133delinsCA
ENST00000589145.1:c.-52-8681_-52-8680delinsTG (CYGB)	ENSP00000468559.1:n.-52-8681_-52-8680delinsTG
ENST00000590555.5:n.445-134_445-133delinsCA (PRCD)
ENST00000592014.5:c.75-134_75-133delinsCA (PRCD)	ENSP00000467661.1:n.75-134_75-133delinsCA
ENST00000592432.5:n.249-134_249-133delinsCA (PRCD)
NM_001077620.2:c.75-134_75-133delinsCA (PRCD)	NP_001071088.1:n.75-134_75-133delinsCA
NR_033357.1:n.249-134_249-133delinsCA (PRCD)
XM_011524272.1:c.-52-8681_-52-8680delinsTG (CYGB)	XP_011522574.1:n.-52-8681_-52-8680delinsTG
XM_011525184.1:c.198-134_198-133delinsCA (PRCD)	XP_011523486.1:n.198-134_198-133delinsCA
XM_017024116.1:c.-52-8681_-52-8680delinsTG (CYGB)	XP_016879605.1:n.-52-8681_-52-8680delinsTG
XM_017025013.1:c.75-134_75-133delinsCA (PRCD)	XP_016880502.1:n.75-134_75-133delinsCA
XM_017025014.1:c.75-134_75-133delinsCA (PRCD)	XP_016880503.1:n.75-134_75-133delinsCA
XM_017025015.1:c.75-134_75-133delinsCA (PRCD)	XP_016880504.1:n.75-134_75-133delinsCA
NM_001077620.3:c.75-134_75-133delinsCA (PRCD) MANE Select	NP_001071088.1:n.75-134_75-133delinsCA
NR_033357.2:n.249-134_249-133delinsCA (PRCD)