Canonical Allele Identifier: CA8729710

Gene: PRKAR1A FAM20A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68539893G>A , CM000679.2:g.68539893G>A	GRCh38
NC_000017.10:g.66536034G>A , CM000679.1:g.66536034G>A	GRCh37
NC_000017.9:g.64047629G>A	NCBI36
NG_007093.3:g.131271G>A , LRG_514:g.131271G>A
NG_029809.1:g.66062C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_017565.4:c.1293C>T (FAM20A) MANE Select	NP_060035.2:p.Asn431=
ENST00000592554.2:c.1293C>T (FAM20A) MANE Select	ENSP00000468308.1:p.Asn431=
NM_001243746.1:c.879C>T (FAM20A)	NP_001230675.1:p.Asn293=
NM_001243746.2:c.879C>T (FAM20A)	NP_001230675.1:p.Asn293=
NM_001276290.1:c.973+9892G>A (PRKAR1A)	NP_001263219.1:n.973+9892G>A
NM_017565.3:c.1293C>T (FAM20A)	NP_060035.2:p.Asn431=
NR_027751.1:n.1008C>T (FAM20A)
NR_027751.2:n.1008C>T (FAM20A)
ENST00000226094.9:n.971C>T (FAM20A)
ENST00000375556.8:n.1394C>T (FAM20A)
ENST00000585981.6:c.973+9892G>A (PRKAR1A)	ENSP00000467311.2:n.973+9892G>A
ENST00000588188.6:c.973+9892G>A (PRKAR1A)	ENSP00000468106.2:n.973+9892G>A
ENST00000588188.7:c.973+9892G>A (PRKAR1A)	ENSP00000468106.2:n.973+9892G>A
ENST00000590074.5:c.1449C>T (FAM20A)
ENST00000590873.5:c.115C>T (FAM20A)	ENSP00000467884.1:n.115C>T
ENST00000592554.1:c.1293C>T (FAM20A)	ENSP00000468308.1:p.Asn431=
ENST00000619787.4:c.105C>T (FAM20A)	ENSP00000481085.1:p.Asn35=
ENST00000711037.1:c.973+9892G>A (PRKAR1A)	ENSP00000518555.1:n.973+9892G>A
XM_006721959.2:c.879C>T (FAM20A)	XP_006722022.1:p.Asn293=
XM_006721959.3:c.879C>T (FAM20A)	XP_006722022.1:p.Asn293=
XM_011524917.1:c.1173C>T (FAM20A)	XP_011523219.1:p.Asn391=
XR_001752544.2:n.1389C>T (FAM20A)
XR_002958041.1:n.1541C>T (FAM20A)
XR_934486.1:n.1598C>T (FAM20A)
XR_934489.1:n.1330C>T (FAM20A)
XR_934490.1:n.1507C>T (FAM20A)