Canonical Allele Identifier: CA2552104697

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401330_127401331insA , CM000670.2:g.127401330_127401331insA GRCh38
NC_000008.10:g.128413575_128413576insA , CM000670.1:g.128413575_128413576insA GRCh37
NC_000008.9:g.128482757_128482758insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13558_-559-13557insA (POU5F1B) ENSP00000495779.1:n.-559-13558_-559-13557insA
NR_109834.1:n.932_933insA (CCAT2)
NR_117100.1:n.1176+19498_1176+19499insT (CASC8)