Canonical Allele Identifier: CA2272264136

Gene: PRKAR1A FAM20A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68540893C= , CM000679.2:g.68540893C=	GRCh38
NC_000017.10:g.66537034C= , CM000679.1:g.66537034C=	GRCh37
NC_000017.9:g.64048629C=	NCBI36
NG_007093.3:g.132271C= , LRG_514:g.132271C=
NG_029809.1:g.65062G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.974-10191C= (PRKAR1A)	ENSP00000468106.2:n.974-10191C=
ENST00000711037.1:c.974-10191C= (PRKAR1A)	ENSP00000518555.1:n.974-10191C=
ENST00000585981.6:c.974-10191C= (PRKAR1A)	ENSP00000467311.2:n.974-10191C=
ENST00000592554.2:c.1175G= (FAM20A) MANE Select	ENSP00000468308.1:p.Arg392=
ENST00000226094.9:n.853G= (FAM20A)
ENST00000375556.8:n.1099G= (FAM20A)
ENST00000588188.6:c.974-10191C= (PRKAR1A)	ENSP00000468106.2:n.974-10191C=
ENST00000590074.5:c.1331G= (FAM20A)
ENST00000590873.5:c.42-927G= (FAM20A)	ENSP00000467884.1:n.42-927G=
ENST00000592554.1:c.1175G= (FAM20A)	ENSP00000468308.1:p.Arg392=
NM_001243746.1:c.761G= (FAM20A)	NP_001230675.1:p.Arg254=
NM_001276290.1:c.974-10191C= (PRKAR1A)	NP_001263219.1:n.974-10191C=
NM_017565.3:c.1175G= (FAM20A)	NP_060035.2:p.Arg392=
NR_027751.1:n.890G= (FAM20A)
XM_006721959.2:c.761G= (FAM20A)	XP_006722022.1:p.Arg254=
XM_006721960.2:c.*39G= (FAM20A)	XP_006722023.1:n.*39G=
XM_011524917.1:c.1055G= (FAM20A)	XP_011523219.1:p.Arg352=
XM_011524921.1:c.*39G= (FAM20A)	XP_011523223.1:n.*39G=
XR_934486.1:n.1303G= (FAM20A)
XR_934487.1:n.1303G= (FAM20A)
XR_934488.1:n.1613G= (FAM20A)
XR_934489.1:n.1212G= (FAM20A)
XR_934490.1:n.1212G= (FAM20A)
XM_006721959.3:c.761G= (FAM20A)	XP_006722022.1:p.Arg254=
XM_011524918.3:c.*664G= (FAM20A)	XP_011523220.1:n.*664G=
XM_017024781.2:c.*542G= (FAM20A)	XP_016880270.1:n.*542G=
XR_001752543.2:n.1488G= (FAM20A)
XR_001752544.2:n.1271G= (FAM20A)
XR_002958041.1:n.1246G= (FAM20A)
XR_934487.3:n.1246G= (FAM20A)
NM_017565.4:c.1175G= (FAM20A) MANE Select	NP_060035.2:p.Arg392=
NM_001243746.2:c.761G= (FAM20A)	NP_001230675.1:p.Arg254=
NR_027751.2:n.890G= (FAM20A)