Canonical Allele Identifier: CA2272265098

Gene: PRKAR1A FAM20A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68542769T= , CM000679.2:g.68542769T=	GRCh38
NC_000017.10:g.66538910T= , CM000679.1:g.66538910T=	GRCh37
NC_000017.9:g.64050505T=	NCBI36
NG_007093.3:g.134147T= , LRG_514:g.134147T=
NG_029809.1:g.63186A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.974-8315T= (PRKAR1A)	ENSP00000468106.2:n.974-8315T=
ENST00000711037.1:c.974-8315T= (PRKAR1A)	ENSP00000518555.1:n.974-8315T=
ENST00000585981.6:c.974-8315T= (PRKAR1A)	ENSP00000467311.2:n.974-8315T=
ENST00000592554.2:c.853A= (FAM20A) MANE Select	ENSP00000468308.1:p.Ile285=
ENST00000226094.9:n.506A= (FAM20A)
ENST00000588188.6:c.974-8315T= (PRKAR1A)	ENSP00000468106.2:n.974-8315T=
ENST00000590074.5:c.1009A= (FAM20A)
ENST00000590873.5:c.41+860A= (FAM20A)	ENSP00000467884.1:n.41+860A=
ENST00000592554.1:c.853A= (FAM20A)	ENSP00000468308.1:p.Ile285=
ENST00000592847.1:n.495A= (FAM20A)
NM_001243746.1:c.439A= (FAM20A)	NP_001230675.1:p.Ile147=
NM_001276290.1:c.974-8315T= (PRKAR1A)	NP_001263219.1:n.974-8315T=
NM_017565.3:c.853A= (FAM20A)	NP_060035.2:p.Ile285=
NR_027751.1:n.543A= (FAM20A)
XM_006721959.2:c.439A= (FAM20A)	XP_006722022.1:p.Ile147=
XM_006721960.2:c.853A= (FAM20A)	XP_006722023.1:p.Ile285=
XM_011524917.1:c.809-604A= (FAM20A)	XP_011523219.1:n.809-604A=
XM_011524918.1:c.853A= (FAM20A)	XP_011523220.1:p.Ile285=
XM_011524919.1:c.813-604A= (FAM20A)	XP_011523221.1:n.813-604A=
XM_011524920.1:c.813-604A= (FAM20A)	XP_011523222.1:n.813-604A=
XM_011524921.1:c.813-604A= (FAM20A)	XP_011523223.1:n.813-604A=
XR_429905.1:n.977A= (FAM20A)
XR_934486.1:n.981A= (FAM20A)
XR_934487.1:n.981A= (FAM20A)
XR_934488.1:n.981A= (FAM20A)
XR_934489.1:n.941-604A= (FAM20A)
XR_934490.1:n.941-604A= (FAM20A)
XM_006721959.3:c.439A= (FAM20A)	XP_006722022.1:p.Ile147=
XM_011524918.3:c.853A= (FAM20A)	XP_011523220.1:p.Ile285=
XM_017024781.2:c.853A= (FAM20A)	XP_016880270.1:p.Ile285=
XR_001752543.2:n.924A= (FAM20A)
XR_001752544.2:n.924A= (FAM20A)
XR_002958041.1:n.924A= (FAM20A)
XR_429905.2:n.920A= (FAM20A)
XR_934487.3:n.924A= (FAM20A)
NM_017565.4:c.853A= (FAM20A) MANE Select	NP_060035.2:p.Ile285=
NM_001243746.2:c.439A= (FAM20A)	NP_001230675.1:p.Ile147=
NR_027751.2:n.543A= (FAM20A)