Canonical Allele Identifier: CA2546772373

Gene: PRKAR1A

Linked Data

• gnomAD v3: 17-68529099-C-CGCCG
• gnomAD v4: 17-68529099-C-CGCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68529099_68529100insGCCG , CM000679.2:g.68529099_68529100insGCCG	GRCh38
NC_000017.10:g.66525240_66525241insGCCG , CM000679.1:g.66525240_66525241insGCCG	GRCh37
NC_000017.9:g.64036835_64036836insGCCG	NCBI36
NG_007093.3:g.120477_120478insGCCG , LRG_514:g.120477_120478insGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.891+108_891+109insGCCG	ENSP00000468106.2:n.891+108_891+109insGCCG
ENST00000711037.1:c.891+108_891+109insGCCG	ENSP00000518555.1:n.891+108_891+109insGCCG
ENST00000585427.6:c.891+108_891+109insGCCG	ENSP00000464715.2:n.891+108_891+109insGCCG
ENST00000585981.6:c.891+108_891+109insGCCG	ENSP00000467311.2:n.891+108_891+109insGCCG
ENST00000588178.6:c.891+108_891+109insGCCG	ENSP00000465013.2:n.891+108_891+109insGCCG
ENST00000589017.6:c.891+108_891+109insGCCG	ENSP00000465445.2:n.891+108_891+109insGCCG
ENST00000589480.6:c.891+108_891+109insGCCG	ENSP00000466649.2:n.891+108_891+109insGCCG
ENST00000592800.6:c.891+108_891+109insGCCG	ENSP00000466314.2:n.891+108_891+109insGCCG
ENST00000686019.1:n.1118_1119insGCCG
ENST00000689501.1:n.3083+108_3083+109insGCCG
ENST00000691392.1:n.1858+108_1858+109insGCCG
ENST00000589228.6:c.891+108_891+109insGCCG MANE Select	ENSP00000464977.2:n.891+108_891+109insGCCG
ENST00000358598.6:c.891+108_891+109insGCCG	ENSP00000351410.1:n.891+108_891+109insGCCG
ENST00000392710.8:c.*506+108_*506+109insGCCG	ENSP00000376474.4:n.*506+108_*506+109insGCCG
ENST00000392711.5:c.891+108_891+109insGCCG	ENSP00000376475.1:n.891+108_891+109insGCCG
ENST00000536854.6:c.891+108_891+109insGCCG	ENSP00000445625.1:n.891+108_891+109insGCCG
ENST00000585907.1:n.439+108_439+109insGCCG
ENST00000586397.5:c.891+108_891+109insGCCG	ENSP00000466459.1:n.891+108_891+109insGCCG
ENST00000586541.5:c.303+108_303+109insGCCG
ENST00000588188.6:c.891+108_891+109insGCCG	ENSP00000468106.2:n.891+108_891+109insGCCG
ENST00000589228.5:c.891+108_891+109insGCCG	ENSP00000464977.1:n.891+108_891+109insGCCG
ENST00000592800.5:c.301+108_301+109insGCCG
NM_001276289.1:c.891+108_891+109insGCCG	NP_001263218.1:n.891+108_891+109insGCCG
NM_001276290.1:c.891+108_891+109insGCCG	NP_001263219.1:n.891+108_891+109insGCCG
NM_001278433.1:c.891+108_891+109insGCCG	NP_001265362.1:n.891+108_891+109insGCCG
NM_002734.4:c.891+108_891+109insGCCG , LRG_514t1:c.891+108_891+109insGCCG	NP_002725.1:n.891+108_891+109insGCCG
NM_212471.2:c.891+108_891+109insGCCG	NP_997636.1:n.891+108_891+109insGCCG
NM_212472.2:c.891+108_891+109insGCCG , LRG_514t2:c.891+108_891+109insGCCG	NP_997637.1:n.891+108_891+109insGCCG
XM_011524983.1:c.891+108_891+109insGCCG	XP_011523285.1:n.891+108_891+109insGCCG
XM_011524984.1:c.891+108_891+109insGCCG	XP_011523286.1:n.891+108_891+109insGCCG
XM_011524985.1:c.891+108_891+109insGCCG	XP_011523287.1:n.891+108_891+109insGCCG
XM_011524983.3:c.891+108_891+109insGCCG	XP_011523285.1:n.891+108_891+109insGCCG
XM_011524984.3:c.891+108_891+109insGCCG	XP_011523286.1:n.891+108_891+109insGCCG
XM_011524985.3:c.891+108_891+109insGCCG	XP_011523287.1:n.891+108_891+109insGCCG
NM_001369389.1:c.891+108_891+109insGCCG	NP_001356318.1:n.891+108_891+109insGCCG
NM_001369390.1:c.891+108_891+109insGCCG	NP_001356319.1:n.891+108_891+109insGCCG
NM_002734.5:c.891+108_891+109insGCCG MANE Select	NP_002725.1:n.891+108_891+109insGCCG
NM_001276289.2:c.891+108_891+109insGCCG	NP_001263218.1:n.891+108_891+109insGCCG
NM_001278433.2:c.891+108_891+109insGCCG	NP_001265362.1:n.891+108_891+109insGCCG
NM_212471.3:c.891+108_891+109insGCCG	NP_997636.1:n.891+108_891+109insGCCG