Canonical Allele Identifier: CA349399525

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296982C>G (hg19) ; chr2:g.178432255C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432255C>G , CM000664.2:g.178432255C>G	GRCh38
NC_000002.11:g.179296982C>G , CM000664.1:g.179296982C>G	GRCh37
NC_000002.10:g.179005228C>G	NCBI36
NG_009053.1:g.23977G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.785-1G>C (PRKRA) MANE Select	ENSP00000318176.4:n.785-1G>C
ENST00000448279.2:c.*513-1G>C (PRKRA)	ENSP00000388455.1:n.*513-1G>C
ENST00000457633.2:c.*289-1G>C (PRKRA)	ENSP00000408668.2:n.*289-1G>C
ENST00000474793.6:n.926-1G>C (PRKRA)
ENST00000676505.1:c.*545-1G>C (PRKRA)	ENSP00000504163.1:n.*545-1G>C
ENST00000676586.1:n.2922-1G>C (PRKRA)
ENST00000676752.1:n.2684-1G>C (PRKRA)
ENST00000676832.1:c.*606-1G>C (PRKRA)	ENSP00000503231.1:n.*606-1G>C
ENST00000676922.1:c.*513-1G>C (PRKRA)	ENSP00000503369.1:n.*513-1G>C
ENST00000677136.1:n.2777-1G>C (PRKRA)
ENST00000677206.1:c.*577-1G>C (PRKRA)	ENSP00000503034.1:n.*577-1G>C
ENST00000677253.1:c.*482-1G>C (PRKRA)	ENSP00000503466.1:n.*482-1G>C
ENST00000677386.1:c.*228-1G>C (PRKRA)	ENSP00000503003.1:n.*228-1G>C
ENST00000677460.1:c.*114-1G>C (PRKRA)	ENSP00000504507.1:n.*114-1G>C
ENST00000677584.1:c.*623-1G>C (PRKRA)	ENSP00000504411.1:n.*623-1G>C
ENST00000677689.1:c.530-1G>C (PRKRA)	ENSP00000502919.1:n.530-1G>C
ENST00000677859.1:c.638-1G>C (PRKRA)
ENST00000677981.1:c.533-1G>C (PRKRA)	ENSP00000503536.1:n.533-1G>C
ENST00000678053.1:c.*545-1G>C (PRKRA)	ENSP00000504330.1:n.*545-1G>C
ENST00000678058.1:c.529-1G>C (PRKRA)	ENSP00000503203.1:n.529-1G>C
ENST00000678167.1:c.*339-1G>C (PRKRA)	ENSP00000504479.1:n.*339-1G>C
ENST00000678775.1:c.446-1G>C (PRKRA)	ENSP00000504030.1:n.446-1G>C
ENST00000678845.1:c.446-1G>C (PRKRA)	ENSP00000503011.1:n.446-1G>C
ENST00000679037.1:c.*453-1G>C (PRKRA)	ENSP00000504421.1:n.*453-1G>C
ENST00000679202.1:n.1872-1G>C (PRKRA)
ENST00000325748.8:c.785-1G>C (PRKRA)	ENSP00000318176.4:n.785-1G>C
ENST00000424699.5:c.*577-1G>C (PRKRA)	ENSP00000408029.1:n.*577-1G>C
ENST00000432031.6:c.752-1G>C (PRKRA)	ENSP00000393883.2:n.752-1G>C
ENST00000487082.5:c.710-1G>C (PRKRA)	ENSP00000430604.1:n.710-1G>C
ENST00000490501.5:n.1012-1G>C (PRKRA)
NM_001139517.1:c.752-1G>C (PRKRA)	NP_001132989.1:n.752-1G>C
NM_001139518.1:c.710-1G>C (PRKRA)	NP_001132990.1:n.710-1G>C
NM_001316362.1:c.446-1G>C (PRKRA)	NP_001303291.1:n.446-1G>C
NM_003690.4:c.785-1G>C (PRKRA)	NP_003681.1:n.785-1G>C
NR_110204.1:n.872-1127C>G (CHROMR)
NR_110205.1:n.716-1127C>G (CHROMR)
NR_110206.1:n.651-1127C>G (CHROMR)
XM_005246921.3:c.446-1G>C (PRKRA)	XP_005246978.1:n.446-1G>C
XM_011512063.1:c.530-1G>C (PRKRA)	XP_011510365.1:n.530-1G>C
XM_011512064.1:c.530-1G>C (PRKRA)	XP_011510366.1:n.530-1G>C
XM_011512066.1:c.446-1G>C (PRKRA)	XP_011510368.1:n.446-1G>C
XM_011512063.2:c.530-1G>C (PRKRA)	XP_011510365.1:n.530-1G>C
XM_011512066.2:c.446-1G>C (PRKRA)	XP_011510368.1:n.446-1G>C
XM_017005159.1:c.446-1G>C (PRKRA)	XP_016860648.1:n.446-1G>C
XR_001739008.2:n.826-1G>C (PRKRA)
NM_003690.5:c.785-1G>C (PRKRA) MANE Select	NP_003681.1:n.785-1G>C
NM_001316362.2:c.446-1G>C (PRKRA)	NP_001303291.1:n.446-1G>C