Canonical Allele Identifier: CA349400902

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179300982T>C (hg19) ; chr2:g.178436255T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178436255T>C , CM000664.2:g.178436255T>C	GRCh38
NC_000002.11:g.179300982T>C , CM000664.1:g.179300982T>C	GRCh37
NC_000002.10:g.179009228T>C	NCBI36
NG_009053.1:g.19977A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.674A>G (PRKRA) MANE Select	ENSP00000318176.4:p.Lys225Arg
ENST00000448279.2:c.*402A>G (PRKRA)	ENSP00000388455.1:n.*402A>G
ENST00000457633.2:c.*178A>G (PRKRA)	ENSP00000408668.2:n.*178A>G
ENST00000474793.6:n.815A>G (PRKRA)
ENST00000676505.1:c.*434A>G (PRKRA)	ENSP00000504163.1:n.*434A>G
ENST00000676586.1:n.2811A>G (PRKRA)
ENST00000676752.1:n.2573A>G (PRKRA)
ENST00000676832.1:c.*495A>G (PRKRA)	ENSP00000503231.1:n.*495A>G
ENST00000676922.1:c.*402A>G (PRKRA)	ENSP00000503369.1:n.*402A>G
ENST00000677136.1:n.2666A>G (PRKRA)
ENST00000677206.1:c.*466A>G (PRKRA)	ENSP00000503034.1:n.*466A>G
ENST00000677253.1:c.*371A>G (PRKRA)	ENSP00000503466.1:n.*371A>G
ENST00000677386.1:c.*117A>G (PRKRA)	ENSP00000503003.1:n.*117A>G
ENST00000677460.1:c.*3A>G (PRKRA)	ENSP00000504507.1:n.*3A>G
ENST00000677584.1:c.*512A>G (PRKRA)	ENSP00000504411.1:n.*512A>G
ENST00000677689.1:c.419A>G (PRKRA)	ENSP00000502919.1:p.Lys140Arg
ENST00000677859.1:c.527A>G (PRKRA)
ENST00000677981.1:c.422A>G (PRKRA)	ENSP00000503536.1:p.Lys141Arg
ENST00000678053.1:c.*434A>G (PRKRA)	ENSP00000504330.1:n.*434A>G
ENST00000678058.1:c.418A>G (PRKRA)	ENSP00000503203.1:n.418A>G
ENST00000678167.1:c.*228A>G (PRKRA)	ENSP00000504479.1:n.*228A>G
ENST00000678775.1:c.335A>G (PRKRA)	ENSP00000504030.1:p.Lys112Arg
ENST00000678845.1:c.335A>G (PRKRA)	ENSP00000503011.1:p.Lys112Arg
ENST00000679037.1:c.*342A>G (PRKRA)	ENSP00000504421.1:n.*342A>G
ENST00000679202.1:n.1761A>G (PRKRA)
ENST00000325748.8:c.674A>G (PRKRA)	ENSP00000318176.4:p.Lys225Arg
ENST00000424699.5:c.*466A>G (PRKRA)	ENSP00000408029.1:n.*466A>G
ENST00000432031.6:c.641A>G (PRKRA)	ENSP00000393883.2:p.Lys214Arg
ENST00000487082.5:c.599A>G (PRKRA)	ENSP00000430604.1:p.Lys200Arg
ENST00000490501.5:n.901A>G (PRKRA)
NM_001139517.1:c.641A>G (PRKRA)	NP_001132989.1:p.Lys214Arg
NM_001139518.1:c.599A>G (PRKRA)	NP_001132990.1:p.Lys200Arg
NM_001316362.1:c.335A>G (PRKRA)	NP_001303291.1:p.Lys112Arg
NM_003690.4:c.674A>G (PRKRA)	NP_003681.1:p.Lys225Arg
NR_110204.1:n.966-2612T>C (CHROMR)
XM_005246921.3:c.335A>G (PRKRA)	XP_005246978.1:p.Lys112Arg
XM_011512063.1:c.419A>G (PRKRA)	XP_011510365.1:p.Lys140Arg
XM_011512064.1:c.419A>G (PRKRA)	XP_011510366.1:p.Lys140Arg
XM_011512066.1:c.335A>G (PRKRA)	XP_011510368.1:p.Lys112Arg
XM_011512063.2:c.419A>G (PRKRA)	XP_011510365.1:p.Lys140Arg
XM_011512066.2:c.335A>G (PRKRA)	XP_011510368.1:p.Lys112Arg
XM_017005159.1:c.335A>G (PRKRA)	XP_016860648.1:p.Lys112Arg
XR_001739008.2:n.715A>G (PRKRA)
NM_003690.5:c.674A>G (PRKRA) MANE Select	NP_003681.1:p.Lys225Arg
NM_001316362.2:c.335A>G (PRKRA)	NP_001303291.1:p.Lys112Arg