Canonical Allele Identifier: CA2346738043
Gene: CDC25B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795448_3795452delinsCAAAG , CM000682.2:g.3795448_3795452delinsCAAAG GRCh38
NC_000020.10:g.3776095_3776099delinsCAAAG , CM000682.1:g.3776095_3776099delinsCAAAG GRCh37
NC_000020.9:g.3724095_3724099delinsCAAAG NCBI36
NG_029040.2:g.13677_13681delinsCAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000344256.10:c.9-2174_9-2170delinsCAAAG ENSP00000339125.6:n.9-2174_9-2170delinsCAAAG
ENST00000379598.9:c.9-2174_9-2170delinsCAAAG ENSP00000368918.5:n.9-2174_9-2170delinsCAAAG
NM_001287516.1:c.9-2174_9-2170delinsCAAAG NP_001274445.1:n.9-2174_9-2170delinsCAAAG
NM_001287517.1:c.9-2216_9-2212delinsCAAAG NP_001274446.1:n.9-2216_9-2212delinsCAAAG
NM_001287518.1:c.9-2174_9-2170delinsCAAAG NP_001274447.1:n.9-2174_9-2170delinsCAAAG
NR_136336.1:n.369-2174_369-2170delinsCAAAG
NM_001287516.2:c.9-2174_9-2170delinsCAAAG NP_001274445.1:n.9-2174_9-2170delinsCAAAG
NM_001287517.2:c.9-2216_9-2212delinsCAAAG NP_001274446.1:n.9-2216_9-2212delinsCAAAG
NM_001287518.2:c.9-2174_9-2170delinsCAAAG NP_001274447.1:n.9-2174_9-2170delinsCAAAG
NR_136336.2:n.190-2174_190-2170delinsCAAAG