Canonical Allele Identifier: CA1818225079
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080044_127080047delinsAAAT , CM000670.2:g.127080044_127080047delinsAAAT GRCh38
NC_000008.10:g.128092289_128092292delinsAAAT , CM000670.1:g.128092289_128092292delinsAAAT GRCh37
NC_000008.9:g.128161471_128161474delinsAAAT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.171_174delinsAAAT (PRNCR1)
NR_119373.1:n.102-914_102-911delinsATTT (PCAT2)