Canonical Allele Identifier: CA8787863

Gene: PRCD CYGB

Linked Data

• dbSNP Id: rs759275085
• ExAC: 17:74536338 G / GCA
• gnomAD v2: 17-74536338-G-GCA
• gnomAD v4: 17-76540256-G-GCA
• MyVariant Identifiers: chr17:g.74536338_74536339insCA (hg19) ; chr17:g.76540256_76540257insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540256_76540257insCA , CM000679.2:g.76540256_76540257insCA	GRCh38
NC_000017.10:g.74536338_74536339insCA , CM000679.1:g.74536338_74536339insCA	GRCh37
NC_000017.9:g.72047933_72047934insCA	NCBI36
NG_016702.1:g.17671_17672insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.74+41_74+42insCA (PRCD) MANE Select	ENSP00000467661.1:n.74+41_74+42insCA
ENST00000397633.7:n.46-249_46-248insCA (PRCD)
ENST00000465808.7:n.93-249_93-248insCA (PRCD)
ENST00000586148.1:c.74+41_74+42insCA (PRCD)	ENSP00000465932.1:n.74+41_74+42insCA
ENST00000589145.1:c.-52-8566_-52-8565insTG (CYGB)	ENSP00000468559.1:n.-52-8566_-52-8565insTG
ENST00000590555.5:n.445-249_445-248insCA (PRCD)
ENST00000592014.5:c.74+41_74+42insCA (PRCD)	ENSP00000467661.1:n.74+41_74+42insCA
ENST00000592432.5:n.249-249_249-248insCA (PRCD)
NM_001077620.2:c.74+41_74+42insCA (PRCD)	NP_001071088.1:n.74+41_74+42insCA
NR_033357.1:n.249-249_249-248insCA (PRCD)
XM_011524272.1:c.-52-8566_-52-8565insTG (CYGB)	XP_011522574.1:n.-52-8566_-52-8565insTG
XM_011525184.1:c.197+41_197+42insCA (PRCD)	XP_011523486.1:n.197+41_197+42insCA
XM_017024116.1:c.-52-8566_-52-8565insTG (CYGB)	XP_016879605.1:n.-52-8566_-52-8565insTG
XM_017025013.1:c.74+41_74+42insCA (PRCD)	XP_016880502.1:n.74+41_74+42insCA
XM_017025014.1:c.74+41_74+42insCA (PRCD)	XP_016880503.1:n.74+41_74+42insCA
XM_017025015.1:c.74+41_74+42insCA (PRCD)	XP_016880504.1:n.74+41_74+42insCA
NM_001077620.3:c.74+41_74+42insCA (PRCD) MANE Select	NP_001071088.1:n.74+41_74+42insCA
NR_033357.2:n.249-249_249-248insCA (PRCD)