Canonical Allele Identifier: CA16044247
Gene: PRKAR1B HGNC NCBI

Linked Data

ClinVar Variation Id: 375411
ClinVar RCV Id: RCV000416507
dbSNP Id: rs1057519490

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.711357A>C , CM000669.2:g.711357A>C GRCh38
NC_000007.13:g.750994A>C , CM000669.1:g.750994A>C GRCh37
NC_000007.12:g.717520A>C NCBI36
NG_042811.1:g.21320T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703505.1:n.196T>G
ENST00000537384.6:c.149T>G MANE Select ENSP00000440449.1:p.Leu50Arg
ENST00000360274.8:c.149T>G ENSP00000353415.4:p.Leu50Arg
ENST00000403562.5:c.149T>G ENSP00000385349.1:p.Leu50Arg
ENST00000406797.5:c.149T>G ENSP00000385749.1:p.Leu50Arg
ENST00000417852.5:c.149T>G ENSP00000406670.1:p.Leu50Arg
ENST00000430040.5:c.149T>G ENSP00000402648.1:p.Leu50Arg
ENST00000456696.2:c.149T>G ENSP00000410414.2:p.Leu50Arg
ENST00000488474.1:n.199T>G
ENST00000537384.5:c.149T>G ENSP00000440449.1:p.Leu50Arg
ENST00000544935.5:c.149T>G ENSP00000444487.1:p.Leu50Arg
NM_001164758.1:c.149T>G NP_001158230.1:p.Leu50Arg
NM_001164759.1:c.149T>G NP_001158231.1:p.Leu50Arg
NM_001164760.1:c.149T>G NP_001158232.1:p.Leu50Arg
NM_001164761.1:c.149T>G NP_001158233.1:p.Leu50Arg
NM_001164762.1:c.149T>G NP_001158234.1:p.Leu50Arg
NM_002735.2:c.149T>G NP_002726.1:p.Leu50Arg
XM_005249809.2:c.149T>G XP_005249866.1:p.Leu50Arg
XM_011515447.1:c.149T>G XP_011513749.1:p.Leu50Arg
NM_001164760.2:c.149T>G MANE Select NP_001158232.1:p.Leu50Arg
NM_001164758.2:c.149T>G NP_001158230.1:p.Leu50Arg
NM_001164761.2:c.149T>G NP_001158233.1:p.Leu50Arg
NM_001164762.2:c.149T>G NP_001158234.1:p.Leu50Arg
NM_002735.3:c.149T>G NP_002726.1:p.Leu50Arg