Canonical Allele Identifier: CA349398702
Gene: PRKRA HGNC NCBI
CHROMR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178432161T>A , CM000664.2:g.178432161T>A GRCh38
NC_000002.11:g.179296888T>A , CM000664.1:g.179296888T>A GRCh37
NC_000002.10:g.179005134T>A NCBI36
NG_009053.1:g.24071A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325748.9:c.878A>T (PRKRA) MANE Select ENSP00000318176.4:p.Asn293Ile
ENST00000448279.2:c.*606A>T (PRKRA) ENSP00000388455.1:n.*606A>T
ENST00000457633.2:c.*382A>T (PRKRA) ENSP00000408668.2:n.*382A>T
ENST00000474793.6:n.1019A>T (PRKRA)
ENST00000676505.1:c.*638A>T (PRKRA) ENSP00000504163.1:n.*638A>T
ENST00000676586.1:n.3015A>T (PRKRA)
ENST00000676752.1:n.2777A>T (PRKRA)
ENST00000676832.1:c.*699A>T (PRKRA) ENSP00000503231.1:n.*699A>T
ENST00000676922.1:c.*606A>T (PRKRA) ENSP00000503369.1:n.*606A>T
ENST00000677136.1:n.2870A>T (PRKRA)
ENST00000677206.1:c.*670A>T (PRKRA) ENSP00000503034.1:n.*670A>T
ENST00000677253.1:c.*575A>T (PRKRA) ENSP00000503466.1:n.*575A>T
ENST00000677386.1:c.*321A>T (PRKRA) ENSP00000503003.1:n.*321A>T
ENST00000677460.1:c.*207A>T (PRKRA) ENSP00000504507.1:n.*207A>T
ENST00000677584.1:c.*716A>T (PRKRA) ENSP00000504411.1:n.*716A>T
ENST00000677689.1:c.623A>T (PRKRA) ENSP00000502919.1:p.Asn208Ile
ENST00000677859.1:c.731A>T (PRKRA)
ENST00000677981.1:c.626A>T (PRKRA) ENSP00000503536.1:p.Asn209Ile
ENST00000678053.1:c.*638A>T (PRKRA) ENSP00000504330.1:n.*638A>T
ENST00000678058.1:c.622A>T (PRKRA) ENSP00000503203.1:n.622A>T
ENST00000678167.1:c.*432A>T (PRKRA) ENSP00000504479.1:n.*432A>T
ENST00000678775.1:c.539A>T (PRKRA) ENSP00000504030.1:p.Asn180Ile
ENST00000678845.1:c.539A>T (PRKRA) ENSP00000503011.1:p.Asn180Ile
ENST00000679037.1:c.*546A>T (PRKRA) ENSP00000504421.1:n.*546A>T
ENST00000679202.1:n.1965A>T (PRKRA)
ENST00000325748.8:c.878A>T (PRKRA) ENSP00000318176.4:p.Asn293Ile
ENST00000424699.5:c.*670A>T (PRKRA) ENSP00000408029.1:n.*670A>T
ENST00000432031.6:c.845A>T (PRKRA) ENSP00000393883.2:p.Asn282Ile
ENST00000487082.5:c.803A>T (PRKRA) ENSP00000430604.1:p.Asn268Ile
ENST00000490501.5:n.1105A>T (PRKRA)
NM_001139517.1:c.845A>T (PRKRA) NP_001132989.1:p.Asn282Ile
NM_001139518.1:c.803A>T (PRKRA) NP_001132990.1:p.Asn268Ile
NM_001316362.1:c.539A>T (PRKRA) NP_001303291.1:p.Asn180Ile
NM_003690.4:c.878A>T (PRKRA) NP_003681.1:p.Asn293Ile
NR_110204.1:n.872-1221T>A (CHROMR)
NR_110205.1:n.716-1221T>A (CHROMR)
NR_110206.1:n.651-1221T>A (CHROMR)
XM_005246921.3:c.539A>T (PRKRA) XP_005246978.1:p.Asn180Ile
XM_011512063.1:c.623A>T (PRKRA) XP_011510365.1:p.Asn208Ile
XM_011512064.1:c.623A>T (PRKRA) XP_011510366.1:p.Asn208Ile
XM_011512066.1:c.539A>T (PRKRA) XP_011510368.1:p.Asn180Ile
XM_011512063.2:c.623A>T (PRKRA) XP_011510365.1:p.Asn208Ile
XM_011512066.2:c.539A>T (PRKRA) XP_011510368.1:p.Asn180Ile
XM_017005159.1:c.539A>T (PRKRA) XP_016860648.1:p.Asn180Ile
XR_001739008.2:n.919A>T (PRKRA)
NM_003690.5:c.878A>T (PRKRA) MANE Select NP_003681.1:p.Asn293Ile
NM_001316362.2:c.539A>T (PRKRA) NP_001303291.1:p.Asn180Ile