Canonical Allele Identifier: CA349398846

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296909C>G (hg19) ; chr2:g.178432182C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432182C>G , CM000664.2:g.178432182C>G	GRCh38
NC_000002.11:g.179296909C>G , CM000664.1:g.179296909C>G	GRCh37
NC_000002.10:g.179005155C>G	NCBI36
NG_009053.1:g.24050G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.857G>C (PRKRA) MANE Select	ENSP00000318176.4:p.Gly286Ala
ENST00000448279.2:c.*585G>C (PRKRA)	ENSP00000388455.1:n.*585G>C
ENST00000457633.2:c.*361G>C (PRKRA)	ENSP00000408668.2:n.*361G>C
ENST00000474793.6:n.998G>C (PRKRA)
ENST00000676505.1:c.*617G>C (PRKRA)	ENSP00000504163.1:n.*617G>C
ENST00000676586.1:n.2994G>C (PRKRA)
ENST00000676752.1:n.2756G>C (PRKRA)
ENST00000676832.1:c.*678G>C (PRKRA)	ENSP00000503231.1:n.*678G>C
ENST00000676922.1:c.*585G>C (PRKRA)	ENSP00000503369.1:n.*585G>C
ENST00000677136.1:n.2849G>C (PRKRA)
ENST00000677206.1:c.*649G>C (PRKRA)	ENSP00000503034.1:n.*649G>C
ENST00000677253.1:c.*554G>C (PRKRA)	ENSP00000503466.1:n.*554G>C
ENST00000677386.1:c.*300G>C (PRKRA)	ENSP00000503003.1:n.*300G>C
ENST00000677460.1:c.*186G>C (PRKRA)	ENSP00000504507.1:n.*186G>C
ENST00000677584.1:c.*695G>C (PRKRA)	ENSP00000504411.1:n.*695G>C
ENST00000677689.1:c.602G>C (PRKRA)	ENSP00000502919.1:p.Gly201Ala
ENST00000677859.1:c.710G>C (PRKRA)
ENST00000677981.1:c.605G>C (PRKRA)	ENSP00000503536.1:p.Gly202Ala
ENST00000678053.1:c.*617G>C (PRKRA)	ENSP00000504330.1:n.*617G>C
ENST00000678058.1:c.601G>C (PRKRA)	ENSP00000503203.1:n.601G>C
ENST00000678167.1:c.*411G>C (PRKRA)	ENSP00000504479.1:n.*411G>C
ENST00000678775.1:c.518G>C (PRKRA)	ENSP00000504030.1:p.Gly173Ala
ENST00000678845.1:c.518G>C (PRKRA)	ENSP00000503011.1:p.Gly173Ala
ENST00000679037.1:c.*525G>C (PRKRA)	ENSP00000504421.1:n.*525G>C
ENST00000679202.1:n.1944G>C (PRKRA)
ENST00000325748.8:c.857G>C (PRKRA)	ENSP00000318176.4:p.Gly286Ala
ENST00000424699.5:c.*649G>C (PRKRA)	ENSP00000408029.1:n.*649G>C
ENST00000432031.6:c.824G>C (PRKRA)	ENSP00000393883.2:p.Gly275Ala
ENST00000487082.5:c.782G>C (PRKRA)	ENSP00000430604.1:p.Gly261Ala
ENST00000490501.5:n.1084G>C (PRKRA)
NM_001139517.1:c.824G>C (PRKRA)	NP_001132989.1:p.Gly275Ala
NM_001139518.1:c.782G>C (PRKRA)	NP_001132990.1:p.Gly261Ala
NM_001316362.1:c.518G>C (PRKRA)	NP_001303291.1:p.Gly173Ala
NM_003690.4:c.857G>C (PRKRA)	NP_003681.1:p.Gly286Ala
NR_110204.1:n.872-1200C>G (CHROMR)
NR_110205.1:n.716-1200C>G (CHROMR)
NR_110206.1:n.651-1200C>G (CHROMR)
XM_005246921.3:c.518G>C (PRKRA)	XP_005246978.1:p.Gly173Ala
XM_011512063.1:c.602G>C (PRKRA)	XP_011510365.1:p.Gly201Ala
XM_011512064.1:c.602G>C (PRKRA)	XP_011510366.1:p.Gly201Ala
XM_011512066.1:c.518G>C (PRKRA)	XP_011510368.1:p.Gly173Ala
XM_011512063.2:c.602G>C (PRKRA)	XP_011510365.1:p.Gly201Ala
XM_011512066.2:c.518G>C (PRKRA)	XP_011510368.1:p.Gly173Ala
XM_017005159.1:c.518G>C (PRKRA)	XP_016860648.1:p.Gly173Ala
XR_001739008.2:n.898G>C (PRKRA)
NM_003690.5:c.857G>C (PRKRA) MANE Select	NP_003681.1:p.Gly286Ala
NM_001316362.2:c.518G>C (PRKRA)	NP_001303291.1:p.Gly173Ala