Canonical Allele Identifier: CA1003892031
Gene: PRKACB HGNC NCBI

Linked Data

dbSNP Id: rs1649299109
gnomAD v3: 1-84100842-GA-G
gnomAD v4: 1-84100842-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84100843del , CM000663.2:g.84100843del GRCh38
NC_000001.10:g.84566526del , CM000663.1:g.84566526del GRCh37
NC_000001.9:g.84339114del NCBI36
NG_029728.1:g.27782del

Transcript Alleles

HGVS Amino-acid change
ENST00000370688.7:c.46+22472del ENSP00000359722.3:n.46+22472del
ENST00000370689.6:c.46+22472del ENSP00000359723.2:n.46+22472del
NM_002731.3:c.46+22472del NP_002722.1:n.46+22472del
NM_207578.2:c.46+22472del NP_997461.1:n.46+22472del
XM_011541764.1:c.46+22472del XP_011540066.1:n.46+22472del
XM_017001713.2:c.46+22472del XP_016857202.1:n.46+22472del
NM_001375576.1:c.46+22472del NP_001362505.1:n.46+22472del
NM_207578.3:c.46+22472del NP_997461.1:n.46+22472del
NM_002731.4:c.46+22472del NP_002722.1:n.46+22472del
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