Canonical Allele Identifier: CA1818352386

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401099_127401104delinsCTTTAT , CM000670.2:g.127401099_127401104delinsCTTTAT GRCh38
NC_000008.10:g.128413344_128413349delinsCTTTAT , CM000670.1:g.128413344_128413349delinsCTTTAT GRCh37
NC_000008.9:g.128482526_128482531delinsCTTTAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13789_-559-13784delinsCTTTAT (POU5F1B) ENSP00000495779.1:n.-559-13789_-559-13784...
NR_109834.1:n.701_706delinsCTTTAT (CCAT2)
NR_117100.1:n.1176+19725_1176+19730delinsATAAAG (CASC8)