Canonical Allele Identifier: CA2272265115

Gene: PRKAR1A FAM20A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68542793G= , CM000679.2:g.68542793G=	GRCh38
NC_000017.10:g.66538934G= , CM000679.1:g.66538934G=	GRCh37
NC_000017.9:g.64050529G=	NCBI36
NG_007093.3:g.134171G= , LRG_514:g.134171G=
NG_029809.1:g.63162C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.974-8291G= (PRKAR1A)	ENSP00000468106.2:n.974-8291G=
ENST00000711037.1:c.974-8291G= (PRKAR1A)	ENSP00000518555.1:n.974-8291G=
ENST00000585981.6:c.974-8291G= (PRKAR1A)	ENSP00000467311.2:n.974-8291G=
ENST00000592554.2:c.829C= (FAM20A) MANE Select	ENSP00000468308.1:p.Arg277=
ENST00000226094.9:n.482C= (FAM20A)
ENST00000588188.6:c.974-8291G= (PRKAR1A)	ENSP00000468106.2:n.974-8291G=
ENST00000590074.5:c.985C= (FAM20A)
ENST00000590873.5:c.41+836C= (FAM20A)	ENSP00000467884.1:n.41+836C=
ENST00000592554.1:c.829C= (FAM20A)	ENSP00000468308.1:p.Arg277=
ENST00000592847.1:n.471C= (FAM20A)
NM_001243746.1:c.415C= (FAM20A)	NP_001230675.1:p.Arg139=
NM_001276290.1:c.974-8291G= (PRKAR1A)	NP_001263219.1:n.974-8291G=
NM_017565.3:c.829C= (FAM20A)	NP_060035.2:p.Arg277=
NR_027751.1:n.519C= (FAM20A)
XM_006721959.2:c.415C= (FAM20A)	XP_006722022.1:p.Arg139=
XM_006721960.2:c.829C= (FAM20A)	XP_006722023.1:p.Arg277=
XM_011524917.1:c.809-628C= (FAM20A)	XP_011523219.1:n.809-628C=
XM_011524918.1:c.829C= (FAM20A)	XP_011523220.1:p.Arg277=
XM_011524919.1:c.813-628C= (FAM20A)	XP_011523221.1:n.813-628C=
XM_011524920.1:c.813-628C= (FAM20A)	XP_011523222.1:n.813-628C=
XM_011524921.1:c.813-628C= (FAM20A)	XP_011523223.1:n.813-628C=
XR_429905.1:n.953C= (FAM20A)
XR_934486.1:n.957C= (FAM20A)
XR_934487.1:n.957C= (FAM20A)
XR_934488.1:n.957C= (FAM20A)
XR_934489.1:n.941-628C= (FAM20A)
XR_934490.1:n.941-628C= (FAM20A)
XM_006721959.3:c.415C= (FAM20A)	XP_006722022.1:p.Arg139=
XM_011524918.3:c.829C= (FAM20A)	XP_011523220.1:p.Arg277=
XM_017024781.2:c.829C= (FAM20A)	XP_016880270.1:p.Arg277=
XR_001752543.2:n.900C= (FAM20A)
XR_001752544.2:n.900C= (FAM20A)
XR_002958041.1:n.900C= (FAM20A)
XR_429905.2:n.896C= (FAM20A)
XR_934487.3:n.900C= (FAM20A)
NM_017565.4:c.829C= (FAM20A) MANE Select	NP_060035.2:p.Arg277=
NM_001243746.2:c.415C= (FAM20A)	NP_001230675.1:p.Arg139=
NR_027751.2:n.519C= (FAM20A)