Canonical Allele Identifier: CA293324169

Gene: PRKAR1A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68512544C>T , CM000679.2:g.68512544C>T	GRCh38
NC_000017.10:g.66508685C>T , CM000679.1:g.66508685C>T	GRCh37
NC_000017.9:g.64020280C>T	NCBI36
NG_007093.3:g.103922C>T , LRG_514:g.103922C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002734.5:c.-11C>T MANE Select	NP_002725.1:n.-11C>T
ENST00000589228.6:c.-11C>T MANE Select	ENSP00000464977.2:n.-11C>T
NM_001276289.1:c.-144C>T	NP_001263218.1:n.-144C>T
NM_001276289.2:c.-144C>T	NP_001263218.1:n.-144C>T
NM_001278433.1:c.-6-2850C>T	NP_001265362.1:n.-6-2850C>T
NM_001278433.2:c.-6-2850C>T	NP_001265362.1:n.-6-2850C>T
NM_001369389.1:c.-140+402C>T	NP_001356318.1:n.-140+402C>T
NM_002734.4:c.-11C>T , LRG_514t1:c.-11C>T	NP_002725.1:n.-11C>T
NM_212471.2:c.-7+402C>T	NP_997636.1:n.-7+402C>T
NM_212471.3:c.-7+402C>T	NP_997636.1:n.-7+402C>T
NM_212472.2:c.-42C>T , LRG_514t2:c.-42C>T	NP_997637.1:n.-42C>T
ENST00000358598.6:c.-7+402C>T	ENSP00000351410.1:n.-7+402C>T
ENST00000392710.8:c.-11C>T	ENSP00000376474.4:n.-11C>T
ENST00000392711.5:c.-42C>T	ENSP00000376475.1:n.-42C>T
ENST00000536854.6:c.-144C>T	ENSP00000445625.1:n.-144C>T
ENST00000585427.5:c.-7+49C>T	ENSP00000464715.1:n.-7+49C>T
ENST00000585427.6:c.-7+49C>T	ENSP00000464715.2:n.-7+49C>T
ENST00000585460.1:n.115C>T
ENST00000585608.5:c.-11C>T	ENSP00000466722.1:n.-11C>T
ENST00000588188.7:c.-11C>T	ENSP00000468106.2:n.-11C>T
ENST00000588702.5:c.-42C>T	ENSP00000464701.1:n.-42C>T
ENST00000589017.5:c.-140+402C>T	ENSP00000465445.1:n.-140+402C>T
ENST00000589017.6:c.-140+402C>T	ENSP00000465445.2:n.-140+402C>T
ENST00000589228.5:c.-11C>T	ENSP00000464977.1:n.-11C>T
ENST00000589309.5:c.-213C>T	ENSP00000467500.1:n.-213C>T
ENST00000592194.1:n.130C>T
ENST00000592800.6:c.-7+402C>T	ENSP00000466314.2:n.-7+402C>T
ENST00000686019.1:n.109C>T
ENST00000691392.1:n.123C>T
XM_011524985.1:c.-140+402C>T	XP_011523287.1:n.-140+402C>T
XM_011524985.3:c.-140+402C>T	XP_011523287.1:n.-140+402C>T