Canonical Allele Identifier: CA2734032699

Gene: PRKAR1A

Linked Data

• dbSNP Id: rs2143368643

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68528994_68528995insCAACGTCGGTC , CM000679.2:g.68528994_68528995insCAACGTCGGTC	GRCh38
NC_000017.10:g.66525135_66525136insCAACGTCGGTC , CM000679.1:g.66525135_66525136insCAACGTCGGTC	GRCh37
NC_000017.9:g.64036730_64036731insCAACGTCGGTC	NCBI36
NG_007093.3:g.120372_120373insCAACGTCGGTC , LRG_514:g.120372_120373insCAACGTCGGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.891+3_891+4insCAACGTCGGTC	ENSP00000468106.2:n.891+3_891+4insCAACGTCGGTC
ENST00000711037.1:c.891+3_891+4insCAACGTCGGTC	ENSP00000518555.1:n.891+3_891+4insCAACGTCGGTC
ENST00000585427.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000464715.2:n.891+3_891+4insCAACGTCGGTC
ENST00000585981.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000467311.2:n.891+3_891+4insCAACGTCGGTC
ENST00000588178.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000465013.2:n.891+3_891+4insCAACGTCGGTC
ENST00000589017.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000465445.2:n.891+3_891+4insCAACGTCGGTC
ENST00000589480.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000466649.2:n.891+3_891+4insCAACGTCGGTC
ENST00000592800.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000466314.2:n.891+3_891+4insCAACGTCGGTC
ENST00000686019.1:n.1013_1014insCAACGTCGGTC
ENST00000689501.1:n.3083+3_3083+4insCAACGTCGGTC
ENST00000691392.1:n.1858+3_1858+4insCAACGTCGGTC
ENST00000589228.6:c.891+3_891+4insCAACGTCGGTC MANE Select	ENSP00000464977.2:n.891+3_891+4insCAACGTCGGTC
ENST00000358598.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000351410.1:n.891+3_891+4insCAACGTCGGTC
ENST00000392710.8:c.*506+3_*506+4insCAACGTCGGTC	ENSP00000376474.4:n.*506+3_*506+4insCAACGTCGGTC
ENST00000392711.5:c.891+3_891+4insCAACGTCGGTC	ENSP00000376475.1:n.891+3_891+4insCAACGTCGGTC
ENST00000536854.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000445625.1:n.891+3_891+4insCAACGTCGGTC
ENST00000585907.1:n.439+3_439+4insCAACGTCGGTC
ENST00000586397.5:c.891+3_891+4insCAACGTCGGTC	ENSP00000466459.1:n.891+3_891+4insCAACGTCGGTC
ENST00000586541.5:c.303+3_303+4insCAACGTCGGTC
ENST00000588188.6:c.891+3_891+4insCAACGTCGGTC	ENSP00000468106.2:n.891+3_891+4insCAACGTCGGTC
ENST00000589228.5:c.891+3_891+4insCAACGTCGGTC	ENSP00000464977.1:n.891+3_891+4insCAACGTCGGTC
ENST00000592800.5:c.301+3_301+4insCAACGTCGGTC
NM_001276289.1:c.891+3_891+4insCAACGTCGGTC	NP_001263218.1:n.891+3_891+4insCAACGTCGGTC
NM_001276290.1:c.891+3_891+4insCAACGTCGGTC	NP_001263219.1:n.891+3_891+4insCAACGTCGGTC
NM_001278433.1:c.891+3_891+4insCAACGTCGGTC	NP_001265362.1:n.891+3_891+4insCAACGTCGGTC
NM_002734.4:c.891+3_891+4insCAACGTCGGTC , LRG_514t1:c.891+3_891+4insCAACGTCGGTC	NP_002725.1:n.891+3_891+4insCAACGTCGGTC
NM_212471.2:c.891+3_891+4insCAACGTCGGTC	NP_997636.1:n.891+3_891+4insCAACGTCGGTC
NM_212472.2:c.891+3_891+4insCAACGTCGGTC , LRG_514t2:c.891+3_891+4insCAACGTCGGTC	NP_997637.1:n.891+3_891+4insCAACGTCGGTC
XM_011524983.1:c.891+3_891+4insCAACGTCGGTC	XP_011523285.1:n.891+3_891+4insCAACGTCGGTC
XM_011524984.1:c.891+3_891+4insCAACGTCGGTC	XP_011523286.1:n.891+3_891+4insCAACGTCGGTC
XM_011524985.1:c.891+3_891+4insCAACGTCGGTC	XP_011523287.1:n.891+3_891+4insCAACGTCGGTC
XM_011524983.3:c.891+3_891+4insCAACGTCGGTC	XP_011523285.1:n.891+3_891+4insCAACGTCGGTC
XM_011524984.3:c.891+3_891+4insCAACGTCGGTC	XP_011523286.1:n.891+3_891+4insCAACGTCGGTC
XM_011524985.3:c.891+3_891+4insCAACGTCGGTC	XP_011523287.1:n.891+3_891+4insCAACGTCGGTC
NM_001369389.1:c.891+3_891+4insCAACGTCGGTC	NP_001356318.1:n.891+3_891+4insCAACGTCGGTC
NM_001369390.1:c.891+3_891+4insCAACGTCGGTC	NP_001356319.1:n.891+3_891+4insCAACGTCGGTC
NM_002734.5:c.891+3_891+4insCAACGTCGGTC MANE Select	NP_002725.1:n.891+3_891+4insCAACGTCGGTC
NM_001276289.2:c.891+3_891+4insCAACGTCGGTC	NP_001263218.1:n.891+3_891+4insCAACGTCGGTC
NM_001278433.2:c.891+3_891+4insCAACGTCGGTC	NP_001265362.1:n.891+3_891+4insCAACGTCGGTC
NM_212471.3:c.891+3_891+4insCAACGTCGGTC	NP_997636.1:n.891+3_891+4insCAACGTCGGTC