Canonical Allele Identifier: CA2272264069
Gene: PRKAR1A HGNC NCBI
FAM20A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.68540805_68540808delinsTAGC , CM000679.2:g.68540805_68540808delinsTAGC GRCh38
NC_000017.10:g.66536946_66536949delinsTAGC , CM000679.1:g.66536946_66536949delinsTAGC GRCh37
NC_000017.9:g.64048541_64048544delinsTAGC NCBI36
NG_007093.3:g.132183_132186delinsTAGC , LRG_514:g.132183_132186delinsTAGC
NG_029809.1:g.65147_65150delinsGCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000588188.7:c.974-10279_974-10276delinsTAGC (PRKAR1A) ENSP00000468106.2:n.974-10279_974-10276delinsTAGC
ENST00000711037.1:c.974-10279_974-10276delinsTAGC (PRKAR1A) ENSP00000518555.1:n.974-10279_974-10276delinsTAGC
ENST00000585981.6:c.974-10279_974-10276delinsTAGC (PRKAR1A) ENSP00000467311.2:n.974-10279_974-10276delinsTAGC
ENST00000592554.2:c.1219+41_1219+44delinsGCTA (FAM20A) MANE Select ENSP00000468308.1:n.1219+41_1219+44delinsGCTA
ENST00000226094.9:n.897+41_897+44delinsGCTA (FAM20A)
ENST00000375556.8:n.1143+41_1143+44delinsGCTA (FAM20A)
ENST00000588188.6:c.974-10279_974-10276delinsTAGC (PRKAR1A) ENSP00000468106.2:n.974-10279_974-10276delinsTAGC
ENST00000590074.5:c.1375+41_1375+44delinsGCTA (FAM20A)
ENST00000590873.5:c.42-842_42-839delinsGCTA (FAM20A) ENSP00000467884.1:n.42-842_42-839delinsGCTA
ENST00000592554.1:c.1219+41_1219+44delinsGCTA (FAM20A) ENSP00000468308.1:n.1219+41_1219+44delinsGCTA
NM_001243746.1:c.805+41_805+44delinsGCTA (FAM20A) NP_001230675.1:n.805+41_805+44delinsGCTA
NM_001276290.1:c.974-10279_974-10276delinsTAGC (PRKAR1A) NP_001263219.1:n.974-10279_974-10276delinsTAGC
NM_017565.3:c.1219+41_1219+44delinsGCTA (FAM20A) NP_060035.2:n.1219+41_1219+44delinsGCTA
NR_027751.1:n.934+41_934+44delinsGCTA (FAM20A)
XM_006721959.2:c.805+41_805+44delinsGCTA (FAM20A) XP_006722022.1:n.805+41_805+44delinsGCTA
XM_011524917.1:c.1099+41_1099+44delinsGCTA (FAM20A) XP_011523219.1:n.1099+41_1099+44delinsGCTA
XR_934486.1:n.1347+41_1347+44delinsGCTA (FAM20A)
XR_934487.1:n.1347+41_1347+44delinsGCTA (FAM20A)
XR_934489.1:n.1256+41_1256+44delinsGCTA (FAM20A)
XR_934490.1:n.1256+41_1256+44delinsGCTA (FAM20A)
XM_006721959.3:c.805+41_805+44delinsGCTA (FAM20A) XP_006722022.1:n.805+41_805+44delinsGCTA
XR_001752544.2:n.1315+41_1315+44delinsGCTA (FAM20A)
XR_002958041.1:n.1290+41_1290+44delinsGCTA (FAM20A)
XR_934487.3:n.1290+41_1290+44delinsGCTA (FAM20A)
NM_017565.4:c.1219+41_1219+44delinsGCTA (FAM20A) MANE Select NP_060035.2:n.1219+41_1219+44delinsGCTA
NM_001243746.2:c.805+41_805+44delinsGCTA (FAM20A) NP_001230675.1:n.805+41_805+44delinsGCTA
NR_027751.2:n.934+41_934+44delinsGCTA (FAM20A)