Canonical Allele Identifier: CA349400924

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179300986C>G (hg19) ; chr2:g.178436259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178436259C>G , CM000664.2:g.178436259C>G	GRCh38
NC_000002.11:g.179300986C>G , CM000664.1:g.179300986C>G	GRCh37
NC_000002.10:g.179009232C>G	NCBI36
NG_009053.1:g.19973G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.670G>C (PRKRA) MANE Select	ENSP00000318176.4:p.Glu224Gln
ENST00000448279.2:c.*398G>C (PRKRA)	ENSP00000388455.1:n.*398G>C
ENST00000457633.2:c.*174G>C (PRKRA)	ENSP00000408668.2:n.*174G>C
ENST00000474793.6:n.811G>C (PRKRA)
ENST00000676505.1:c.*430G>C (PRKRA)	ENSP00000504163.1:n.*430G>C
ENST00000676586.1:n.2807G>C (PRKRA)
ENST00000676752.1:n.2569G>C (PRKRA)
ENST00000676832.1:c.*491G>C (PRKRA)	ENSP00000503231.1:n.*491G>C
ENST00000676922.1:c.*398G>C (PRKRA)	ENSP00000503369.1:n.*398G>C
ENST00000677136.1:n.2662G>C (PRKRA)
ENST00000677206.1:c.*462G>C (PRKRA)	ENSP00000503034.1:n.*462G>C
ENST00000677253.1:c.*367G>C (PRKRA)	ENSP00000503466.1:n.*367G>C
ENST00000677386.1:c.*113G>C (PRKRA)	ENSP00000503003.1:n.*113G>C
ENST00000677460.1:c.575G>C (PRKRA)	ENSP00000504507.1:p.Ter192Ser
ENST00000677584.1:c.*508G>C (PRKRA)	ENSP00000504411.1:n.*508G>C
ENST00000677689.1:c.415G>C (PRKRA)	ENSP00000502919.1:p.Glu139Gln
ENST00000677859.1:c.523G>C (PRKRA)
ENST00000677981.1:c.418G>C (PRKRA)	ENSP00000503536.1:p.Glu140Gln
ENST00000678053.1:c.*430G>C (PRKRA)	ENSP00000504330.1:n.*430G>C
ENST00000678058.1:c.414G>C (PRKRA)	ENSP00000503203.1:n.414G>C
ENST00000678167.1:c.*224G>C (PRKRA)	ENSP00000504479.1:n.*224G>C
ENST00000678775.1:c.331G>C (PRKRA)	ENSP00000504030.1:p.Glu111Gln
ENST00000678845.1:c.331G>C (PRKRA)	ENSP00000503011.1:p.Glu111Gln
ENST00000679037.1:c.*338G>C (PRKRA)	ENSP00000504421.1:n.*338G>C
ENST00000679202.1:n.1757G>C (PRKRA)
ENST00000325748.8:c.670G>C (PRKRA)	ENSP00000318176.4:p.Glu224Gln
ENST00000424699.5:c.*462G>C (PRKRA)	ENSP00000408029.1:n.*462G>C
ENST00000432031.6:c.637G>C (PRKRA)	ENSP00000393883.2:p.Glu213Gln
ENST00000487082.5:c.595G>C (PRKRA)	ENSP00000430604.1:p.Glu199Gln
ENST00000490501.5:n.897G>C (PRKRA)
NM_001139517.1:c.637G>C (PRKRA)	NP_001132989.1:p.Glu213Gln
NM_001139518.1:c.595G>C (PRKRA)	NP_001132990.1:p.Glu199Gln
NM_001316362.1:c.331G>C (PRKRA)	NP_001303291.1:p.Glu111Gln
NM_003690.4:c.670G>C (PRKRA)	NP_003681.1:p.Glu224Gln
NR_110204.1:n.966-2608C>G (CHROMR)
XM_005246921.3:c.331G>C (PRKRA)	XP_005246978.1:p.Glu111Gln
XM_011512063.1:c.415G>C (PRKRA)	XP_011510365.1:p.Glu139Gln
XM_011512064.1:c.415G>C (PRKRA)	XP_011510366.1:p.Glu139Gln
XM_011512066.1:c.331G>C (PRKRA)	XP_011510368.1:p.Glu111Gln
XM_011512063.2:c.415G>C (PRKRA)	XP_011510365.1:p.Glu139Gln
XM_011512066.2:c.331G>C (PRKRA)	XP_011510368.1:p.Glu111Gln
XM_017005159.1:c.331G>C (PRKRA)	XP_016860648.1:p.Glu111Gln
XR_001739008.2:n.711G>C (PRKRA)
NM_003690.5:c.670G>C (PRKRA) MANE Select	NP_003681.1:p.Glu224Gln
NM_001316362.2:c.331G>C (PRKRA)	NP_001303291.1:p.Glu111Gln