Canonical Allele Identifier: CA2272264134

Gene: PRKAR1A FAM20A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68540891G= , CM000679.2:g.68540891G=	GRCh38
NC_000017.10:g.66537032G= , CM000679.1:g.66537032G=	GRCh37
NC_000017.9:g.64048627G=	NCBI36
NG_007093.3:g.132269G= , LRG_514:g.132269G=
NG_029809.1:g.65064C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.974-10193G= (PRKAR1A)	ENSP00000468106.2:n.974-10193G=
ENST00000711037.1:c.974-10193G= (PRKAR1A)	ENSP00000518555.1:n.974-10193G=
ENST00000585981.6:c.974-10193G= (PRKAR1A)	ENSP00000467311.2:n.974-10193G=
ENST00000592554.2:c.1177C= (FAM20A) MANE Select	ENSP00000468308.1:p.Leu393=
ENST00000226094.9:n.855C= (FAM20A)
ENST00000375556.8:n.1101C= (FAM20A)
ENST00000588188.6:c.974-10193G= (PRKAR1A)	ENSP00000468106.2:n.974-10193G=
ENST00000590074.5:c.1333C= (FAM20A)
ENST00000590873.5:c.42-925C= (FAM20A)	ENSP00000467884.1:n.42-925C=
ENST00000592554.1:c.1177C= (FAM20A)	ENSP00000468308.1:p.Leu393=
NM_001243746.1:c.763C= (FAM20A)	NP_001230675.1:p.Leu255=
NM_001276290.1:c.974-10193G= (PRKAR1A)	NP_001263219.1:n.974-10193G=
NM_017565.3:c.1177C= (FAM20A)	NP_060035.2:p.Leu393=
NR_027751.1:n.892C= (FAM20A)
XM_006721959.2:c.763C= (FAM20A)	XP_006722022.1:p.Leu255=
XM_006721960.2:c.*41C= (FAM20A)	XP_006722023.1:n.*41C=
XM_011524917.1:c.1057C= (FAM20A)	XP_011523219.1:p.Leu353=
XM_011524921.1:c.*41C= (FAM20A)	XP_011523223.1:n.*41C=
XR_934486.1:n.1305C= (FAM20A)
XR_934487.1:n.1305C= (FAM20A)
XR_934488.1:n.1615C= (FAM20A)
XR_934489.1:n.1214C= (FAM20A)
XR_934490.1:n.1214C= (FAM20A)
XM_006721959.3:c.763C= (FAM20A)	XP_006722022.1:p.Leu255=
XM_011524918.3:c.*666C= (FAM20A)	XP_011523220.1:n.*666C=
XM_017024781.2:c.*544C= (FAM20A)	XP_016880270.1:n.*544C=
XR_001752543.2:n.1490C= (FAM20A)
XR_001752544.2:n.1273C= (FAM20A)
XR_002958041.1:n.1248C= (FAM20A)
XR_934487.3:n.1248C= (FAM20A)
NM_017565.4:c.1177C= (FAM20A) MANE Select	NP_060035.2:p.Leu393=
NM_001243746.2:c.763C= (FAM20A)	NP_001230675.1:p.Leu255=
NR_027751.2:n.892C= (FAM20A)