Canonical Allele Identifier: CA400757757

Gene: PRKAR1A FAM20A

Linked Data

• MyVariant Identifiers: chr17:g.66537032G>C (hg19) ; chr17:g.68540891G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.68540891G>C , CM000679.2:g.68540891G>C	GRCh38
NC_000017.10:g.66537032G>C , CM000679.1:g.66537032G>C	GRCh37
NC_000017.9:g.64048627G>C	NCBI36
NG_007093.3:g.132269G>C , LRG_514:g.132269G>C
NG_029809.1:g.65064C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588188.7:c.974-10193G>C (PRKAR1A)	ENSP00000468106.2:n.974-10193G>C
ENST00000711037.1:c.974-10193G>C (PRKAR1A)	ENSP00000518555.1:n.974-10193G>C
ENST00000585981.6:c.974-10193G>C (PRKAR1A)	ENSP00000467311.2:n.974-10193G>C
ENST00000592554.2:c.1177C>G (FAM20A) MANE Select	ENSP00000468308.1:p.Leu393Val
ENST00000226094.9:n.855C>G (FAM20A)
ENST00000375556.8:n.1101C>G (FAM20A)
ENST00000588188.6:c.974-10193G>C (PRKAR1A)	ENSP00000468106.2:n.974-10193G>C
ENST00000590074.5:c.1333C>G (FAM20A)
ENST00000590873.5:c.42-925C>G (FAM20A)	ENSP00000467884.1:n.42-925C>G
ENST00000592554.1:c.1177C>G (FAM20A)	ENSP00000468308.1:p.Leu393Val
NM_001243746.1:c.763C>G (FAM20A)	NP_001230675.1:p.Leu255Val
NM_001276290.1:c.974-10193G>C (PRKAR1A)	NP_001263219.1:n.974-10193G>C
NM_017565.3:c.1177C>G (FAM20A)	NP_060035.2:p.Leu393Val
NR_027751.1:n.892C>G (FAM20A)
XM_006721959.2:c.763C>G (FAM20A)	XP_006722022.1:p.Leu255Val
XM_006721960.2:c.*41C>G (FAM20A)	XP_006722023.1:n.*41C>G
XM_011524917.1:c.1057C>G (FAM20A)	XP_011523219.1:p.Leu353Val
XM_011524921.1:c.*41C>G (FAM20A)	XP_011523223.1:n.*41C>G
XR_934486.1:n.1305C>G (FAM20A)
XR_934487.1:n.1305C>G (FAM20A)
XR_934488.1:n.1615C>G (FAM20A)
XR_934489.1:n.1214C>G (FAM20A)
XR_934490.1:n.1214C>G (FAM20A)
XM_006721959.3:c.763C>G (FAM20A)	XP_006722022.1:p.Leu255Val
XM_011524918.3:c.*666C>G (FAM20A)	XP_011523220.1:n.*666C>G
XM_017024781.2:c.*544C>G (FAM20A)	XP_016880270.1:n.*544C>G
XR_001752543.2:n.1490C>G (FAM20A)
XR_001752544.2:n.1273C>G (FAM20A)
XR_002958041.1:n.1248C>G (FAM20A)
XR_934487.3:n.1248C>G (FAM20A)
NM_017565.4:c.1177C>G (FAM20A) MANE Select	NP_060035.2:p.Leu393Val
NM_001243746.2:c.763C>G (FAM20A)	NP_001230675.1:p.Leu255Val
NR_027751.2:n.892C>G (FAM20A)