Canonical Allele Identifier: CA293304294

Gene: PRKAR1A FAM20A

Linked Data

• dbSNP Id: rs901355197
• MyVariant Identifiers: chr17:g.66536934A>T (hg19) ; chr17:g.68540793A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68540793A>T , CM000679.2:g.68540793A>T	GRCh38
NC_000017.10:g.66536934A>T , CM000679.1:g.66536934A>T	GRCh37
NC_000017.9:g.64048529A>T	NCBI36
NG_007093.3:g.132171A>T , LRG_514:g.132171A>T
NG_029809.1:g.65162T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000588188.7:c.974-10291A>T (PRKAR1A)	ENSP00000468106.2:n.974-10291A>T
ENST00000711037.1:c.974-10291A>T (PRKAR1A)	ENSP00000518555.1:n.974-10291A>T
ENST00000585981.6:c.974-10291A>T (PRKAR1A)	ENSP00000467311.2:n.974-10291A>T
ENST00000592554.2:c.1219+56T>A (FAM20A) MANE Select	ENSP00000468308.1:n.1219+56T>A
ENST00000226094.9:n.897+56T>A (FAM20A)
ENST00000375556.8:n.1143+56T>A (FAM20A)
ENST00000588188.6:c.974-10291A>T (PRKAR1A)	ENSP00000468106.2:n.974-10291A>T
ENST00000590074.5:c.1375+56T>A (FAM20A)
ENST00000590873.5:c.42-827T>A (FAM20A)	ENSP00000467884.1:n.42-827T>A
ENST00000592554.1:c.1219+56T>A (FAM20A)	ENSP00000468308.1:n.1219+56T>A
NM_001243746.1:c.805+56T>A (FAM20A)	NP_001230675.1:n.805+56T>A
NM_001276290.1:c.974-10291A>T (PRKAR1A)	NP_001263219.1:n.974-10291A>T
NM_017565.3:c.1219+56T>A (FAM20A)	NP_060035.2:n.1219+56T>A
NR_027751.1:n.934+56T>A (FAM20A)
XM_006721959.2:c.805+56T>A (FAM20A)	XP_006722022.1:n.805+56T>A
XM_011524917.1:c.1099+56T>A (FAM20A)	XP_011523219.1:n.1099+56T>A
XR_934486.1:n.1347+56T>A (FAM20A)
XR_934487.1:n.1347+56T>A (FAM20A)
XR_934489.1:n.1256+56T>A (FAM20A)
XR_934490.1:n.1256+56T>A (FAM20A)
XM_006721959.3:c.805+56T>A (FAM20A)	XP_006722022.1:n.805+56T>A
XR_001752544.2:n.1315+56T>A (FAM20A)
XR_002958041.1:n.1290+56T>A (FAM20A)
XR_934487.3:n.1290+56T>A (FAM20A)
NM_017565.4:c.1219+56T>A (FAM20A) MANE Select	NP_060035.2:n.1219+56T>A
NM_001243746.2:c.805+56T>A (FAM20A)	NP_001230675.1:n.805+56T>A
NR_027751.2:n.934+56T>A (FAM20A)