Canonical Allele Identifier: CA349399348

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296961G>C (hg19) ; chr2:g.178432234G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432234G>C , CM000664.2:g.178432234G>C	GRCh38
NC_000002.11:g.179296961G>C , CM000664.1:g.179296961G>C	GRCh37
NC_000002.10:g.179005207G>C	NCBI36
NG_009053.1:g.23998C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.805C>G (PRKRA) MANE Select	ENSP00000318176.4:p.Gln269Glu
ENST00000448279.2:c.*533C>G (PRKRA)	ENSP00000388455.1:n.*533C>G
ENST00000457633.2:c.*309C>G (PRKRA)	ENSP00000408668.2:n.*309C>G
ENST00000474793.6:n.946C>G (PRKRA)
ENST00000676505.1:c.*565C>G (PRKRA)	ENSP00000504163.1:n.*565C>G
ENST00000676586.1:n.2942C>G (PRKRA)
ENST00000676752.1:n.2704C>G (PRKRA)
ENST00000676832.1:c.*626C>G (PRKRA)	ENSP00000503231.1:n.*626C>G
ENST00000676922.1:c.*533C>G (PRKRA)	ENSP00000503369.1:n.*533C>G
ENST00000677136.1:n.2797C>G (PRKRA)
ENST00000677206.1:c.*597C>G (PRKRA)	ENSP00000503034.1:n.*597C>G
ENST00000677253.1:c.*502C>G (PRKRA)	ENSP00000503466.1:n.*502C>G
ENST00000677386.1:c.*248C>G (PRKRA)	ENSP00000503003.1:n.*248C>G
ENST00000677460.1:c.*134C>G (PRKRA)	ENSP00000504507.1:n.*134C>G
ENST00000677584.1:c.*643C>G (PRKRA)	ENSP00000504411.1:n.*643C>G
ENST00000677689.1:c.550C>G (PRKRA)	ENSP00000502919.1:p.Gln184Glu
ENST00000677859.1:c.658C>G (PRKRA)
ENST00000677981.1:c.553C>G (PRKRA)	ENSP00000503536.1:p.Gln185Glu
ENST00000678053.1:c.*565C>G (PRKRA)	ENSP00000504330.1:n.*565C>G
ENST00000678058.1:c.549C>G (PRKRA)	ENSP00000503203.1:n.549C>G
ENST00000678167.1:c.*359C>G (PRKRA)	ENSP00000504479.1:n.*359C>G
ENST00000678775.1:c.466C>G (PRKRA)	ENSP00000504030.1:p.Gln156Glu
ENST00000678845.1:c.466C>G (PRKRA)	ENSP00000503011.1:p.Gln156Glu
ENST00000679037.1:c.*473C>G (PRKRA)	ENSP00000504421.1:n.*473C>G
ENST00000679202.1:n.1892C>G (PRKRA)
ENST00000325748.8:c.805C>G (PRKRA)	ENSP00000318176.4:p.Gln269Glu
ENST00000424699.5:c.*597C>G (PRKRA)	ENSP00000408029.1:n.*597C>G
ENST00000432031.6:c.772C>G (PRKRA)	ENSP00000393883.2:p.Gln258Glu
ENST00000487082.5:c.730C>G (PRKRA)	ENSP00000430604.1:p.Gln244Glu
ENST00000490501.5:n.1032C>G (PRKRA)
NM_001139517.1:c.772C>G (PRKRA)	NP_001132989.1:p.Gln258Glu
NM_001139518.1:c.730C>G (PRKRA)	NP_001132990.1:p.Gln244Glu
NM_001316362.1:c.466C>G (PRKRA)	NP_001303291.1:p.Gln156Glu
NM_003690.4:c.805C>G (PRKRA)	NP_003681.1:p.Gln269Glu
NR_110204.1:n.872-1148G>C (CHROMR)
NR_110205.1:n.716-1148G>C (CHROMR)
NR_110206.1:n.651-1148G>C (CHROMR)
XM_005246921.3:c.466C>G (PRKRA)	XP_005246978.1:p.Gln156Glu
XM_011512063.1:c.550C>G (PRKRA)	XP_011510365.1:p.Gln184Glu
XM_011512064.1:c.550C>G (PRKRA)	XP_011510366.1:p.Gln184Glu
XM_011512066.1:c.466C>G (PRKRA)	XP_011510368.1:p.Gln156Glu
XM_011512063.2:c.550C>G (PRKRA)	XP_011510365.1:p.Gln184Glu
XM_011512066.2:c.466C>G (PRKRA)	XP_011510368.1:p.Gln156Glu
XM_017005159.1:c.466C>G (PRKRA)	XP_016860648.1:p.Gln156Glu
XR_001739008.2:n.846C>G (PRKRA)
NM_003690.5:c.805C>G (PRKRA) MANE Select	NP_003681.1:p.Gln269Glu
NM_001316362.2:c.466C>G (PRKRA)	NP_001303291.1:p.Gln156Glu