Canonical Allele Identifier: CA1014891782
Gene: CDC25B HGNC NCBI

Linked Data

dbSNP Id: rs2089004585

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795469_3795471del , CM000682.2:g.3795469_3795471del GRCh38
NC_000020.10:g.3776116_3776118del , CM000682.1:g.3776116_3776118del GRCh37
NC_000020.9:g.3724116_3724118del NCBI36
NG_029040.2:g.13698_13700del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344256.10:c.9-2153_9-2151del ENSP00000339125.6:n.9-2153_9-2151del
ENST00000379598.9:c.9-2153_9-2151del ENSP00000368918.5:n.9-2153_9-2151del
NM_001287516.1:c.9-2153_9-2151del NP_001274445.1:n.9-2153_9-2151del
NM_001287517.1:c.9-2195_9-2193del NP_001274446.1:n.9-2195_9-2193del
NM_001287518.1:c.9-2153_9-2151del NP_001274447.1:n.9-2153_9-2151del
NR_136336.1:n.369-2153_369-2151del
NM_001287516.2:c.9-2153_9-2151del NP_001274445.1:n.9-2153_9-2151del
NM_001287517.2:c.9-2195_9-2193del NP_001274446.1:n.9-2195_9-2193del
NM_001287518.2:c.9-2153_9-2151del NP_001274447.1:n.9-2153_9-2151del
NR_136336.2:n.190-2153_190-2151del