Canonical Allele Identifier: CA1143145450
Gene: PRKACB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84100931T= , CM000663.2:g.84100931T= GRCh38
NC_000001.10:g.84566614T= , CM000663.1:g.84566614T= GRCh37
NC_000001.9:g.84339202T= NCBI36
NG_029728.1:g.27870T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370688.7:c.46+22560T= ENSP00000359722.3:n.46+22560T=
ENST00000370689.6:c.46+22560T= ENSP00000359723.2:n.46+22560T=
NM_002731.3:c.46+22560T= NP_002722.1:n.46+22560T=
NM_207578.2:c.46+22560T= NP_997461.1:n.46+22560T=
XM_011541764.1:c.46+22560T= XP_011540066.1:n.46+22560T=
XM_017001713.2:c.46+22560T= XP_016857202.1:n.46+22560T=
NM_001375576.1:c.46+22560T= NP_001362505.1:n.46+22560T=
NM_207578.3:c.46+22560T= NP_997461.1:n.46+22560T=
NM_002731.4:c.46+22560T= NP_002722.1:n.46+22560T=