Canonical Allele Identifier: CA2272259675

Gene: PRKAR1A FAM20A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68531401G= , CM000679.2:g.68531401G=	GRCh38
NC_000017.10:g.66527542G= , CM000679.1:g.66527542G=	GRCh37
NC_000017.9:g.64039137G=	NCBI36
NG_007093.3:g.122779G= , LRG_514:g.122779G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.973+1400G= (PRKAR1A)	ENSP00000468106.2:n.973+1400G=
ENST00000711037.1:c.973+1400G= (PRKAR1A)	ENSP00000518555.1:n.973+1400G=
ENST00000585427.6:c.*952G= (PRKAR1A)	ENSP00000464715.2:n.*952G=
ENST00000585981.6:c.973+1400G= (PRKAR1A)	ENSP00000467311.2:n.973+1400G=
ENST00000588178.6:c.*952G= (PRKAR1A)	ENSP00000465013.2:n.*952G=
ENST00000589017.6:c.*952G= (PRKAR1A)	ENSP00000465445.2:n.*952G=
ENST00000589480.6:c.*952G= (PRKAR1A)	ENSP00000466649.2:n.*952G=
ENST00000592800.6:c.*1323G= (PRKAR1A)	ENSP00000466314.2:n.*1323G=
ENST00000686019.1:n.3145G= (PRKAR1A)
ENST00000689501.1:n.4290G= (PRKAR1A)
ENST00000691392.1:n.3065G= (PRKAR1A)
ENST00000589228.6:c.*952G= (PRKAR1A) MANE Select	ENSP00000464977.2:n.*952G=
ENST00000358598.6:c.*952G= (PRKAR1A)	ENSP00000351410.1:n.*952G=
ENST00000392710.8:c.*1713G= (PRKAR1A)	ENSP00000376474.4:n.*1713G=
ENST00000392711.5:c.*952G= (PRKAR1A)	ENSP00000376475.1:n.*952G=
ENST00000536854.6:c.*952G= (PRKAR1A)	ENSP00000445625.1:n.*952G=
ENST00000588188.6:c.973+1400G= (PRKAR1A)	ENSP00000468106.2:n.973+1400G=
ENST00000589228.5:c.*952G= (PRKAR1A)	ENSP00000464977.1:n.*952G=
NM_001276289.1:c.*952G= (PRKAR1A)	NP_001263218.1:n.*952G=
NM_001276290.1:c.973+1400G= (PRKAR1A)	NP_001263219.1:n.973+1400G=
NM_001278433.1:c.*952G= (PRKAR1A)	NP_001265362.1:n.*952G=
NM_002734.4:c.*952G= , LRG_514t1:c.*952G= (PRKAR1A)	NP_002725.1:n.*952G=
NM_212471.2:c.*952G= (PRKAR1A)	NP_997636.1:n.*952G=
NM_212472.2:c.*952G= , LRG_514t2:c.*952G= (PRKAR1A)	NP_997637.1:n.*952G=
XM_011524983.1:c.*952G= (PRKAR1A)	XP_011523285.1:n.*952G=
XM_011524984.1:c.*952G= (PRKAR1A)	XP_011523286.1:n.*952G=
XM_011524985.1:c.*952G= (PRKAR1A)	XP_011523287.1:n.*952G=
XM_006721959.3:c.*6076C= (FAM20A)	XP_006722022.1:n.*6076C=
XM_011524983.3:c.*952G= (PRKAR1A)	XP_011523285.1:n.*952G=
XM_011524984.3:c.*952G= (PRKAR1A)	XP_011523286.1:n.*952G=
XM_011524985.3:c.*952G= (PRKAR1A)	XP_011523287.1:n.*952G=
XR_001752544.2:n.7798C= (FAM20A)
XR_002958041.1:n.7950C= (FAM20A)
NM_001369389.1:c.*952G= (PRKAR1A)	NP_001356318.1:n.*952G=
NM_001369390.1:c.*952G= (PRKAR1A)	NP_001356319.1:n.*952G=
NM_002734.5:c.*952G= (PRKAR1A) MANE Select	NP_002725.1:n.*952G=
NM_001276289.2:c.*952G= (PRKAR1A)	NP_001263218.1:n.*952G=
NM_001278433.2:c.*952G= (PRKAR1A)	NP_001265362.1:n.*952G=
NM_212471.3:c.*952G= (PRKAR1A)	NP_997636.1:n.*952G=