Canonical Allele Identifier: CA739632726

Gene: PRKACB

Linked Data

• dbSNP Id: rs1251821020
• MyVariant Identifiers: chr1:g.84566487_84566488del (hg19) ; chr1:g.84100804_84100805del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84100805_84100806del , CM000663.2:g.84100805_84100806del	GRCh38
NC_000001.10:g.84566488_84566489del , CM000663.1:g.84566488_84566489del	GRCh37
NC_000001.9:g.84339076_84339077del	NCBI36
NG_029728.1:g.27744_27745del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370688.7:c.46+22434_46+22435del	ENSP00000359722.3:n.46+22434_46+22435del
ENST00000370689.6:c.46+22434_46+22435del	ENSP00000359723.2:n.46+22434_46+22435del
NM_002731.3:c.46+22434_46+22435del	NP_002722.1:n.46+22434_46+22435del
NM_207578.2:c.46+22434_46+22435del	NP_997461.1:n.46+22434_46+22435del
XM_011541764.1:c.46+22434_46+22435del	XP_011540066.1:n.46+22434_46+22435del
XM_017001713.2:c.46+22434_46+22435del	XP_016857202.1:n.46+22434_46+22435del
NM_001375576.1:c.46+22434_46+22435del	NP_001362505.1:n.46+22434_46+22435del
NM_207578.3:c.46+22434_46+22435del	NP_997461.1:n.46+22434_46+22435del
NM_002731.4:c.46+22434_46+22435del	NP_002722.1:n.46+22434_46+22435del