Canonical Allele Identifier: CA2810474816

Gene: PRCD CYGB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540256_76540257insCGAGA , CM000679.2:g.76540256_76540257insCGAGA	GRCh38
NC_000017.10:g.74536338_74536339insCGAGA , CM000679.1:g.74536338_74536339insCGAGA	GRCh37
NC_000017.9:g.72047933_72047934insCGAGA	NCBI36
NG_016702.1:g.17671_17672insCGAGA

Transcript Alleles

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