Canonical Allele Identifier: CA430089878

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296944A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432217A>C , CM000664.2:g.178432217A>C	GRCh38
NC_000002.11:g.179296944A>C , CM000664.1:g.179296944A>C	GRCh37
NC_000002.10:g.179005190A>C	NCBI36
NG_009053.1:g.24015T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.822T>G (PRKRA) MANE Select	ENSP00000318176.4:p.Ala274=
ENST00000448279.2:c.*550T>G (PRKRA)	ENSP00000388455.1:n.*550T>G
ENST00000457633.2:c.*326T>G (PRKRA)	ENSP00000408668.2:n.*326T>G
ENST00000474793.6:n.963T>G (PRKRA)
ENST00000676505.1:c.*582T>G (PRKRA)	ENSP00000504163.1:n.*582T>G
ENST00000676586.1:n.2959T>G (PRKRA)
ENST00000676752.1:n.2721T>G (PRKRA)
ENST00000676832.1:c.*643T>G (PRKRA)	ENSP00000503231.1:n.*643T>G
ENST00000676922.1:c.*550T>G (PRKRA)	ENSP00000503369.1:n.*550T>G
ENST00000677136.1:n.2814T>G (PRKRA)
ENST00000677206.1:c.*614T>G (PRKRA)	ENSP00000503034.1:n.*614T>G
ENST00000677253.1:c.*519T>G (PRKRA)	ENSP00000503466.1:n.*519T>G
ENST00000677386.1:c.*265T>G (PRKRA)	ENSP00000503003.1:n.*265T>G
ENST00000677460.1:c.*151T>G (PRKRA)	ENSP00000504507.1:n.*151T>G
ENST00000677584.1:c.*660T>G (PRKRA)	ENSP00000504411.1:n.*660T>G
ENST00000677689.1:c.567T>G (PRKRA)	ENSP00000502919.1:p.Ala189=
ENST00000677859.1:c.675T>G (PRKRA)
ENST00000677981.1:c.570T>G (PRKRA)	ENSP00000503536.1:p.Ala190=
ENST00000678053.1:c.*582T>G (PRKRA)	ENSP00000504330.1:n.*582T>G
ENST00000678058.1:c.566T>G (PRKRA)	ENSP00000503203.1:n.566T>G
ENST00000678167.1:c.*376T>G (PRKRA)	ENSP00000504479.1:n.*376T>G
ENST00000678775.1:c.483T>G (PRKRA)	ENSP00000504030.1:p.Ala161=
ENST00000678845.1:c.483T>G (PRKRA)	ENSP00000503011.1:p.Ala161=
ENST00000679037.1:c.*490T>G (PRKRA)	ENSP00000504421.1:n.*490T>G
ENST00000679202.1:n.1909T>G (PRKRA)
ENST00000325748.8:c.822T>G (PRKRA)	ENSP00000318176.4:p.Ala274=
ENST00000424699.5:c.*614T>G (PRKRA)	ENSP00000408029.1:n.*614T>G
ENST00000432031.6:c.789T>G (PRKRA)	ENSP00000393883.2:p.Ala263=
ENST00000487082.5:c.747T>G (PRKRA)	ENSP00000430604.1:p.Ala249=
ENST00000490501.5:n.1049T>G (PRKRA)
NM_001139517.1:c.789T>G (PRKRA)	NP_001132989.1:p.Ala263=
NM_001139518.1:c.747T>G (PRKRA)	NP_001132990.1:p.Ala249=
NM_001316362.1:c.483T>G (PRKRA)	NP_001303291.1:p.Ala161=
NM_003690.4:c.822T>G (PRKRA)	NP_003681.1:p.Ala274=
NR_110204.1:n.872-1165A>C (CHROMR)
NR_110205.1:n.716-1165A>C (CHROMR)
NR_110206.1:n.651-1165A>C (CHROMR)
XM_005246921.3:c.483T>G (PRKRA)	XP_005246978.1:p.Ala161=
XM_011512063.1:c.567T>G (PRKRA)	XP_011510365.1:p.Ala189=
XM_011512064.1:c.567T>G (PRKRA)	XP_011510366.1:p.Ala189=
XM_011512066.1:c.483T>G (PRKRA)	XP_011510368.1:p.Ala161=
XM_011512063.2:c.567T>G (PRKRA)	XP_011510365.1:p.Ala189=
XM_011512066.2:c.483T>G (PRKRA)	XP_011510368.1:p.Ala161=
XM_017005159.1:c.483T>G (PRKRA)	XP_016860648.1:p.Ala161=
XR_001739008.2:n.863T>G (PRKRA)
NM_003690.5:c.822T>G (PRKRA) MANE Select	NP_003681.1:p.Ala274=
NM_001316362.2:c.483T>G (PRKRA)	NP_001303291.1:p.Ala161=