Canonical Allele Identifier: CA2501928854

Gene: PRKAR1A

Linked Data

• gnomAD v3: 17-68529092-T-TC
• gnomAD v4: 17-68529092-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68529092_68529093insC , CM000679.2:g.68529092_68529093insC	GRCh38
NC_000017.10:g.66525233_66525234insC , CM000679.1:g.66525233_66525234insC	GRCh37
NC_000017.9:g.64036828_64036829insC	NCBI36
NG_007093.3:g.120470_120471insC , LRG_514:g.120470_120471insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.891+101_891+102insC	ENSP00000468106.2:n.891+101_891+102insC
ENST00000711037.1:c.891+101_891+102insC	ENSP00000518555.1:n.891+101_891+102insC
ENST00000585427.6:c.891+101_891+102insC	ENSP00000464715.2:n.891+101_891+102insC
ENST00000585981.6:c.891+101_891+102insC	ENSP00000467311.2:n.891+101_891+102insC
ENST00000588178.6:c.891+101_891+102insC	ENSP00000465013.2:n.891+101_891+102insC
ENST00000589017.6:c.891+101_891+102insC	ENSP00000465445.2:n.891+101_891+102insC
ENST00000589480.6:c.891+101_891+102insC	ENSP00000466649.2:n.891+101_891+102insC
ENST00000592800.6:c.891+101_891+102insC	ENSP00000466314.2:n.891+101_891+102insC
ENST00000686019.1:n.1111_1112insC
ENST00000689501.1:n.3083+101_3083+102insC
ENST00000691392.1:n.1858+101_1858+102insC
ENST00000589228.6:c.891+101_891+102insC MANE Select	ENSP00000464977.2:n.891+101_891+102insC
ENST00000358598.6:c.891+101_891+102insC	ENSP00000351410.1:n.891+101_891+102insC
ENST00000392710.8:c.*506+101_*506+102insC	ENSP00000376474.4:n.*506+101_*506+102insC
ENST00000392711.5:c.891+101_891+102insC	ENSP00000376475.1:n.891+101_891+102insC
ENST00000536854.6:c.891+101_891+102insC	ENSP00000445625.1:n.891+101_891+102insC
ENST00000585907.1:n.439+101_439+102insC
ENST00000586397.5:c.891+101_891+102insC	ENSP00000466459.1:n.891+101_891+102insC
ENST00000586541.5:c.303+101_303+102insC
ENST00000588188.6:c.891+101_891+102insC	ENSP00000468106.2:n.891+101_891+102insC
ENST00000589228.5:c.891+101_891+102insC	ENSP00000464977.1:n.891+101_891+102insC
ENST00000592800.5:c.301+101_301+102insC
NM_001276289.1:c.891+101_891+102insC	NP_001263218.1:n.891+101_891+102insC
NM_001276290.1:c.891+101_891+102insC	NP_001263219.1:n.891+101_891+102insC
NM_001278433.1:c.891+101_891+102insC	NP_001265362.1:n.891+101_891+102insC
NM_002734.4:c.891+101_891+102insC , LRG_514t1:c.891+101_891+102insC	NP_002725.1:n.891+101_891+102insC
NM_212471.2:c.891+101_891+102insC	NP_997636.1:n.891+101_891+102insC
NM_212472.2:c.891+101_891+102insC , LRG_514t2:c.891+101_891+102insC	NP_997637.1:n.891+101_891+102insC
XM_011524983.1:c.891+101_891+102insC	XP_011523285.1:n.891+101_891+102insC
XM_011524984.1:c.891+101_891+102insC	XP_011523286.1:n.891+101_891+102insC
XM_011524985.1:c.891+101_891+102insC	XP_011523287.1:n.891+101_891+102insC
XM_011524983.3:c.891+101_891+102insC	XP_011523285.1:n.891+101_891+102insC
XM_011524984.3:c.891+101_891+102insC	XP_011523286.1:n.891+101_891+102insC
XM_011524985.3:c.891+101_891+102insC	XP_011523287.1:n.891+101_891+102insC
NM_001369389.1:c.891+101_891+102insC	NP_001356318.1:n.891+101_891+102insC
NM_001369390.1:c.891+101_891+102insC	NP_001356319.1:n.891+101_891+102insC
NM_002734.5:c.891+101_891+102insC MANE Select	NP_002725.1:n.891+101_891+102insC
NM_001276289.2:c.891+101_891+102insC	NP_001263218.1:n.891+101_891+102insC
NM_001278433.2:c.891+101_891+102insC	NP_001265362.1:n.891+101_891+102insC
NM_212471.3:c.891+101_891+102insC	NP_997636.1:n.891+101_891+102insC