Canonical Allele Identifier: CA400757755
Gene: PRKAR1A HGNC NCBI
FAM20A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.68540890A>T , CM000679.2:g.68540890A>T GRCh38
NC_000017.10:g.66537031A>T , CM000679.1:g.66537031A>T GRCh37
NC_000017.9:g.64048626A>T NCBI36
NG_007093.3:g.132268A>T , LRG_514:g.132268A>T
NG_029809.1:g.65065T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000588188.7:c.974-10194A>T (PRKAR1A) ENSP00000468106.2:n.974-10194A>T
ENST00000711037.1:c.974-10194A>T (PRKAR1A) ENSP00000518555.1:n.974-10194A>T
ENST00000585981.6:c.974-10194A>T (PRKAR1A) ENSP00000467311.2:n.974-10194A>T
ENST00000592554.2:c.1178T>A (FAM20A) MANE Select ENSP00000468308.1:p.Leu393His
ENST00000226094.9:n.856T>A (FAM20A)
ENST00000375556.8:n.1102T>A (FAM20A)
ENST00000588188.6:c.974-10194A>T (PRKAR1A) ENSP00000468106.2:n.974-10194A>T
ENST00000590074.5:c.1334T>A (FAM20A)
ENST00000590873.5:c.42-924T>A (FAM20A) ENSP00000467884.1:n.42-924T>A
ENST00000592554.1:c.1178T>A (FAM20A) ENSP00000468308.1:p.Leu393His
NM_001243746.1:c.764T>A (FAM20A) NP_001230675.1:p.Leu255His
NM_001276290.1:c.974-10194A>T (PRKAR1A) NP_001263219.1:n.974-10194A>T
NM_017565.3:c.1178T>A (FAM20A) NP_060035.2:p.Leu393His
NR_027751.1:n.893T>A (FAM20A)
XM_006721959.2:c.764T>A (FAM20A) XP_006722022.1:p.Leu255His
XM_006721960.2:c.*42T>A (FAM20A) XP_006722023.1:n.*42T>A
XM_011524917.1:c.1058T>A (FAM20A) XP_011523219.1:p.Leu353His
XM_011524921.1:c.*42T>A (FAM20A) XP_011523223.1:n.*42T>A
XR_934486.1:n.1306T>A (FAM20A)
XR_934487.1:n.1306T>A (FAM20A)
XR_934488.1:n.1616T>A (FAM20A)
XR_934489.1:n.1215T>A (FAM20A)
XR_934490.1:n.1215T>A (FAM20A)
XM_006721959.3:c.764T>A (FAM20A) XP_006722022.1:p.Leu255His
XM_011524918.3:c.*667T>A (FAM20A) XP_011523220.1:n.*667T>A
XM_017024781.2:c.*545T>A (FAM20A) XP_016880270.1:n.*545T>A
XR_001752543.2:n.1491T>A (FAM20A)
XR_001752544.2:n.1274T>A (FAM20A)
XR_002958041.1:n.1249T>A (FAM20A)
XR_934487.3:n.1249T>A (FAM20A)
NM_017565.4:c.1178T>A (FAM20A) MANE Select NP_060035.2:p.Leu393His
NM_001243746.2:c.764T>A (FAM20A) NP_001230675.1:p.Leu255His
NR_027751.2:n.893T>A (FAM20A)