Canonical Allele Identifier: CA2272265088

Gene: PRKAR1A FAM20A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68542736_68542737delinsTG , CM000679.2:g.68542736_68542737delinsTG	GRCh38
NC_000017.10:g.66538877_66538878delinsTG , CM000679.1:g.66538877_66538878delinsTG	GRCh37
NC_000017.9:g.64050472_64050473delinsTG	NCBI36
NG_007093.3:g.134114_134115delinsTG , LRG_514:g.134114_134115delinsTG
NG_029809.1:g.63218_63219delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588188.7:c.974-8348_974-8347delinsTG (PRKAR1A)	ENSP00000468106.2:n.974-8348_974-8347delinsTG
ENST00000711037.1:c.974-8348_974-8347delinsTG (PRKAR1A)	ENSP00000518555.1:n.974-8348_974-8347delinsTG
ENST00000585981.6:c.974-8348_974-8347delinsTG (PRKAR1A)	ENSP00000467311.2:n.974-8348_974-8347delinsTG
ENST00000592554.2:c.885_886delinsCA (FAM20A) MANE Select	ENSP00000468308.1:p.Val295=
ENST00000226094.9:n.538_539delinsCA (FAM20A)
ENST00000588188.6:c.974-8348_974-8347delinsTG (PRKAR1A)	ENSP00000468106.2:n.974-8348_974-8347delinsTG
ENST00000590074.5:c.1041_1042delinsCA (FAM20A)
ENST00000590873.5:c.41+892_41+893delinsCA (FAM20A)	ENSP00000467884.1:n.41+892_41+893delinsCA
ENST00000592554.1:c.885_886delinsCA (FAM20A)	ENSP00000468308.1:p.Val295=
ENST00000592847.1:n.527_528delinsCA (FAM20A)
NM_001243746.1:c.471_472delinsCA (FAM20A)	NP_001230675.1:p.Val157=
NM_001276290.1:c.974-8348_974-8347delinsTG (PRKAR1A)	NP_001263219.1:n.974-8348_974-8347delinsTG
NM_017565.3:c.885_886delinsCA (FAM20A)	NP_060035.2:p.Val295=
NR_027751.1:n.575_576delinsCA (FAM20A)
XM_006721959.2:c.471_472delinsCA (FAM20A)	XP_006722022.1:p.Val157=
XM_006721960.2:c.885_886delinsCA (FAM20A)	XP_006722023.1:p.Val295=
XM_011524917.1:c.809-572_809-571delinsCA (FAM20A)	XP_011523219.1:n.809-572_809-571delinsCA
XM_011524918.1:c.885_886delinsCA (FAM20A)	XP_011523220.1:p.Val295=
XM_011524919.1:c.813-572_813-571delinsCA (FAM20A)	XP_011523221.1:n.813-572_813-571delinsCA
XM_011524920.1:c.813-572_813-571delinsCA (FAM20A)	XP_011523222.1:n.813-572_813-571delinsCA
XM_011524921.1:c.813-572_813-571delinsCA (FAM20A)	XP_011523223.1:n.813-572_813-571delinsCA
XR_429905.1:n.1009_1010delinsCA (FAM20A)
XR_934486.1:n.1013_1014delinsCA (FAM20A)
XR_934487.1:n.1013_1014delinsCA (FAM20A)
XR_934488.1:n.1013_1014delinsCA (FAM20A)
XR_934489.1:n.941-572_941-571delinsCA (FAM20A)
XR_934490.1:n.941-572_941-571delinsCA (FAM20A)
XM_006721959.3:c.471_472delinsCA (FAM20A)	XP_006722022.1:p.Val157=
XM_011524918.3:c.885_886delinsCA (FAM20A)	XP_011523220.1:p.Val295=
XM_017024781.2:c.885_886delinsCA (FAM20A)	XP_016880270.1:p.Val295=
XR_001752543.2:n.956_957delinsCA (FAM20A)
XR_001752544.2:n.956_957delinsCA (FAM20A)
XR_002958041.1:n.956_957delinsCA (FAM20A)
XR_429905.2:n.952_953delinsCA (FAM20A)
XR_934487.3:n.956_957delinsCA (FAM20A)
NM_017565.4:c.885_886delinsCA (FAM20A) MANE Select	NP_060035.2:p.Val295=
NM_001243746.2:c.471_472delinsCA (FAM20A)	NP_001230675.1:p.Val157=
NR_027751.2:n.575_576delinsCA (FAM20A)