Canonical Allele Identifier: CA1818352475

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401164_127401165delinsAG , CM000670.2:g.127401164_127401165delinsAG GRCh38
NC_000008.10:g.128413409_128413410delinsAG , CM000670.1:g.128413409_128413410delinsAG GRCh37
NC_000008.9:g.128482591_128482592delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13724_-559-13723delinsAG (POU5F1B) ENSP00000495779.1:n.-559-13724_-559-13723delinsAG
NR_109834.1:n.766_767delinsAG (CCAT2)
NR_117100.1:n.1176+19664_1176+19665delinsCT (CASC8)