Canonical Allele Identifier: CA2272264140

Gene: PRKAR1A FAM20A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68540899_68540902delinsCTGT , CM000679.2:g.68540899_68540902delinsCTGT	GRCh38
NC_000017.10:g.66537040_66537043delinsCTGT , CM000679.1:g.66537040_66537043delinsCTGT	GRCh37
NC_000017.9:g.64048635_64048638delinsCTGT	NCBI36
NG_007093.3:g.132277_132280delinsCTGT , LRG_514:g.132277_132280delinsCTGT
NG_029809.1:g.65053_65056delinsACAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000588188.7:c.974-10185_974-10182delinsCTGT (PRKAR1A)	ENSP00000468106.2:n.974-10185_974-10182delinsCTGT
ENST00000711037.1:c.974-10185_974-10182delinsCTGT (PRKAR1A)	ENSP00000518555.1:n.974-10185_974-10182delinsCTGT
ENST00000585981.6:c.974-10185_974-10182delinsCTGT (PRKAR1A)	ENSP00000467311.2:n.974-10185_974-10182delinsCTGT
ENST00000592554.2:c.1166_1169delinsACAG (FAM20A) MANE Select	ENSP00000468308.1:p.Asn389=
ENST00000226094.9:n.844_847delinsACAG (FAM20A)
ENST00000375556.8:n.1090_1093delinsACAG (FAM20A)
ENST00000588188.6:c.974-10185_974-10182delinsCTGT (PRKAR1A)	ENSP00000468106.2:n.974-10185_974-10182delinsCTGT
ENST00000590074.5:c.1322_1325delinsACAG (FAM20A)
ENST00000590873.5:c.42-936_42-933delinsACAG (FAM20A)	ENSP00000467884.1:n.42-936_42-933delinsACAG
ENST00000592554.1:c.1166_1169delinsACAG (FAM20A)	ENSP00000468308.1:p.Asn389=
NM_001243746.1:c.752_755delinsACAG (FAM20A)	NP_001230675.1:p.Asn251=
NM_001276290.1:c.974-10185_974-10182delinsCTGT (PRKAR1A)	NP_001263219.1:n.974-10185_974-10182delinsCTGT
NM_017565.3:c.1166_1169delinsACAG (FAM20A)	NP_060035.2:p.Asn389=
NR_027751.1:n.881_884delinsACAG (FAM20A)
XM_006721959.2:c.752_755delinsACAG (FAM20A)	XP_006722022.1:p.Asn251=
XM_006721960.2:c.*30_*33delinsACAG (FAM20A)	XP_006722023.1:n.*30_*33delinsACAG
XM_011524917.1:c.1046_1049delinsACAG (FAM20A)	XP_011523219.1:p.Asn349=
XM_011524918.1:c.*655_*658delinsACAG (FAM20A)	XP_011523220.1:n.*655_*658delinsACAG
XM_011524919.1:c.*1008_*1011delinsACAG (FAM20A)	XP_011523221.1:n.*1008_*1011delinsACAG
XM_011524920.1:c.*611_*614delinsACAG (FAM20A)	XP_011523222.1:n.*611_*614delinsACAG
XM_011524921.1:c.*30_*33delinsACAG (FAM20A)	XP_011523223.1:n.*30_*33delinsACAG
XR_934486.1:n.1294_1297delinsACAG (FAM20A)
XR_934487.1:n.1294_1297delinsACAG (FAM20A)
XR_934488.1:n.1604_1607delinsACAG (FAM20A)
XR_934489.1:n.1203_1206delinsACAG (FAM20A)
XR_934490.1:n.1203_1206delinsACAG (FAM20A)
XM_006721959.3:c.752_755delinsACAG (FAM20A)	XP_006722022.1:p.Asn251=
XM_011524918.3:c.*655_*658delinsACAG (FAM20A)	XP_011523220.1:n.*655_*658delinsACAG
XM_017024781.2:c.*533_*536delinsACAG (FAM20A)	XP_016880270.1:n.*533_*536delinsACAG
XR_001752543.2:n.1479_1482delinsACAG (FAM20A)
XR_001752544.2:n.1262_1265delinsACAG (FAM20A)
XR_002958041.1:n.1237_1240delinsACAG (FAM20A)
XR_934487.3:n.1237_1240delinsACAG (FAM20A)
NM_017565.4:c.1166_1169delinsACAG (FAM20A) MANE Select	NP_060035.2:p.Asn389=
NM_001243746.2:c.752_755delinsACAG (FAM20A)	NP_001230675.1:p.Asn251=
NR_027751.2:n.881_884delinsACAG (FAM20A)