Canonical Allele Identifier: CA986412666

Linked Data

dbSNP Id: rs2074974709

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76540270_76540271insGGGGGGGGG , CM000679.2:g.76540270_76540271insGGGGGGGGG GRCh38
NC_000017.10:g.74536352_74536353insGGGGGGGGG , CM000679.1:g.74536352_74536353insGGGGGGGGG GRCh37
NC_000017.9:g.72047947_72047948insGGGGGGGGG NCBI36
NG_016702.1:g.17685_17686insGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000592014.6:c.74+55_74+56insGGGGGGGGG (PRCD) MANE Select ENSP00000467661.1:n.74+55_74+56insGGGGGGGGG
ENST00000397633.7:n.46-235_46-234insGGGGGGGGG (PRCD)
ENST00000465808.7:n.93-235_93-234insGGGGGGGGG (PRCD)
ENST00000586148.1:c.74+55_74+56insGGGGGGGGG (PRCD) ENSP00000465932.1:n.74+55_74+56insGGGGGGGGG
ENST00000589145.1:c.-52-8576_-52-8575insCCCCCCCCC (CYGB) ENSP00000468559.1:n.-52-8576_-52-8575insCCCCCCCCC
ENST00000590555.5:n.445-235_445-234insGGGGGGGGG (PRCD)
ENST00000592014.5:c.74+55_74+56insGGGGGGGGG (PRCD) ENSP00000467661.1:n.74+55_74+56insGGGGGGGGG
ENST00000592432.5:n.249-235_249-234insGGGGGGGGG (PRCD)
NM_001077620.2:c.74+55_74+56insGGGGGGGGG (PRCD) NP_001071088.1:n.74+55_74+56insGGGGGGGGG
NR_033357.1:n.249-235_249-234insGGGGGGGGG (PRCD)
XM_011524272.1:c.-52-8576_-52-8575insCCCCCCCCC (CYGB) XP_011522574.1:n.-52-8576_-52-8575insCCCCCCCCC
XM_011525184.1:c.197+55_197+56insGGGGGGGGG (PRCD) XP_011523486.1:n.197+55_197+56insGGGGGGGGG
XM_017024116.1:c.-52-8576_-52-8575insCCCCCCCCC (CYGB) XP_016879605.1:n.-52-8576_-52-8575insCCCCCCCCC
XM_017025013.1:c.74+55_74+56insGGGGGGGGG (PRCD) XP_016880502.1:n.74+55_74+56insGGGGGGGGG
XM_017025014.1:c.74+55_74+56insGGGGGGGGG (PRCD) XP_016880503.1:n.74+55_74+56insGGGGGGGGG
XM_017025015.1:c.74+55_74+56insGGGGGGGGG (PRCD) XP_016880504.1:n.74+55_74+56insGGGGGGGGG
NM_001077620.3:c.74+55_74+56insGGGGGGGGG (PRCD) MANE Select NP_001071088.1:n.74+55_74+56insGGGGGGGGG
NR_033357.2:n.249-235_249-234insGGGGGGGGG (PRCD)