Canonical Allele Identifier: CA2639521542
Gene: PRKAR1A HGNC NCBI
FAM20A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.68542838G>T , CM000679.2:g.68542838G>T GRCh38
NC_000017.10:g.66538979G>T , CM000679.1:g.66538979G>T GRCh37
NC_000017.9:g.64050574G>T NCBI36
NG_007093.3:g.134216G>T , LRG_514:g.134216G>T
NG_029809.1:g.63117C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000588188.7:c.974-8246G>T (PRKAR1A) ENSP00000468106.2:n.974-8246G>T
ENST00000711037.1:c.974-8246G>T (PRKAR1A) ENSP00000518555.1:n.974-8246G>T
ENST00000585981.6:c.974-8246G>T (PRKAR1A) ENSP00000467311.2:n.974-8246G>T
ENST00000592554.2:c.813-29C>A (FAM20A) MANE Select ENSP00000468308.1:n.813-29C>A
ENST00000226094.9:n.466-29C>A (FAM20A)
ENST00000588188.6:c.974-8246G>T (PRKAR1A) ENSP00000468106.2:n.974-8246G>T
ENST00000590074.5:c.969-29C>A (FAM20A)
ENST00000590873.5:c.41+791C>A (FAM20A) ENSP00000467884.1:n.41+791C>A
ENST00000592554.1:c.813-29C>A (FAM20A) ENSP00000468308.1:n.813-29C>A
ENST00000592847.1:n.455-29C>A (FAM20A)
NM_001243746.1:c.399-29C>A (FAM20A) NP_001230675.1:n.399-29C>A
NM_001276290.1:c.974-8246G>T (PRKAR1A) NP_001263219.1:n.974-8246G>T
NM_017565.3:c.813-29C>A (FAM20A) NP_060035.2:n.813-29C>A
NR_027751.1:n.503-29C>A (FAM20A)
XM_006721959.2:c.399-29C>A (FAM20A) XP_006722022.1:n.399-29C>A
XM_006721960.2:c.813-29C>A (FAM20A) XP_006722023.1:n.813-29C>A
XM_011524917.1:c.809-673C>A (FAM20A) XP_011523219.1:n.809-673C>A
XM_011524918.1:c.813-29C>A (FAM20A) XP_011523220.1:n.813-29C>A
XM_011524919.1:c.813-673C>A (FAM20A) XP_011523221.1:n.813-673C>A
XM_011524920.1:c.813-673C>A (FAM20A) XP_011523222.1:n.813-673C>A
XM_011524921.1:c.813-673C>A (FAM20A) XP_011523223.1:n.813-673C>A
XR_429905.1:n.937-29C>A (FAM20A)
XR_934486.1:n.941-29C>A (FAM20A)
XR_934487.1:n.941-29C>A (FAM20A)
XR_934488.1:n.941-29C>A (FAM20A)
XR_934489.1:n.941-673C>A (FAM20A)
XR_934490.1:n.941-673C>A (FAM20A)
XM_006721959.3:c.399-29C>A (FAM20A) XP_006722022.1:n.399-29C>A
XM_011524918.3:c.813-29C>A (FAM20A) XP_011523220.1:n.813-29C>A
XM_017024781.2:c.813-29C>A (FAM20A) XP_016880270.1:n.813-29C>A
XR_001752543.2:n.884-29C>A (FAM20A)
XR_001752544.2:n.884-29C>A (FAM20A)
XR_002958041.1:n.884-29C>A (FAM20A)
XR_429905.2:n.880-29C>A (FAM20A)
XR_934487.3:n.884-29C>A (FAM20A)
NM_017565.4:c.813-29C>A (FAM20A) MANE Select NP_060035.2:n.813-29C>A
NM_001243746.2:c.399-29C>A (FAM20A) NP_001230675.1:n.399-29C>A
NR_027751.2:n.503-29C>A (FAM20A)