Canonical Allele Identifier: CA430089882

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296947A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432220A>G , CM000664.2:g.178432220A>G	GRCh38
NC_000002.11:g.179296947A>G , CM000664.1:g.179296947A>G	GRCh37
NC_000002.10:g.179005193A>G	NCBI36
NG_009053.1:g.24012T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.819T>C (PRKRA) MANE Select	ENSP00000318176.4:p.Leu273=
ENST00000448279.2:c.*547T>C (PRKRA)	ENSP00000388455.1:n.*547T>C
ENST00000457633.2:c.*323T>C (PRKRA)	ENSP00000408668.2:n.*323T>C
ENST00000474793.6:n.960T>C (PRKRA)
ENST00000676505.1:c.*579T>C (PRKRA)	ENSP00000504163.1:n.*579T>C
ENST00000676586.1:n.2956T>C (PRKRA)
ENST00000676752.1:n.2718T>C (PRKRA)
ENST00000676832.1:c.*640T>C (PRKRA)	ENSP00000503231.1:n.*640T>C
ENST00000676922.1:c.*547T>C (PRKRA)	ENSP00000503369.1:n.*547T>C
ENST00000677136.1:n.2811T>C (PRKRA)
ENST00000677206.1:c.*611T>C (PRKRA)	ENSP00000503034.1:n.*611T>C
ENST00000677253.1:c.*516T>C (PRKRA)	ENSP00000503466.1:n.*516T>C
ENST00000677386.1:c.*262T>C (PRKRA)	ENSP00000503003.1:n.*262T>C
ENST00000677460.1:c.*148T>C (PRKRA)	ENSP00000504507.1:n.*148T>C
ENST00000677584.1:c.*657T>C (PRKRA)	ENSP00000504411.1:n.*657T>C
ENST00000677689.1:c.564T>C (PRKRA)	ENSP00000502919.1:p.Leu188=
ENST00000677859.1:c.672T>C (PRKRA)
ENST00000677981.1:c.567T>C (PRKRA)	ENSP00000503536.1:p.Leu189=
ENST00000678053.1:c.*579T>C (PRKRA)	ENSP00000504330.1:n.*579T>C
ENST00000678058.1:c.563T>C (PRKRA)	ENSP00000503203.1:n.563T>C
ENST00000678167.1:c.*373T>C (PRKRA)	ENSP00000504479.1:n.*373T>C
ENST00000678775.1:c.480T>C (PRKRA)	ENSP00000504030.1:p.Leu160=
ENST00000678845.1:c.480T>C (PRKRA)	ENSP00000503011.1:p.Leu160=
ENST00000679037.1:c.*487T>C (PRKRA)	ENSP00000504421.1:n.*487T>C
ENST00000679202.1:n.1906T>C (PRKRA)
ENST00000325748.8:c.819T>C (PRKRA)	ENSP00000318176.4:p.Leu273=
ENST00000424699.5:c.*611T>C (PRKRA)	ENSP00000408029.1:n.*611T>C
ENST00000432031.6:c.786T>C (PRKRA)	ENSP00000393883.2:p.Leu262=
ENST00000487082.5:c.744T>C (PRKRA)	ENSP00000430604.1:p.Leu248=
ENST00000490501.5:n.1046T>C (PRKRA)
NM_001139517.1:c.786T>C (PRKRA)	NP_001132989.1:p.Leu262=
NM_001139518.1:c.744T>C (PRKRA)	NP_001132990.1:p.Leu248=
NM_001316362.1:c.480T>C (PRKRA)	NP_001303291.1:p.Leu160=
NM_003690.4:c.819T>C (PRKRA)	NP_003681.1:p.Leu273=
NR_110204.1:n.872-1162A>G (CHROMR)
NR_110205.1:n.716-1162A>G (CHROMR)
NR_110206.1:n.651-1162A>G (CHROMR)
XM_005246921.3:c.480T>C (PRKRA)	XP_005246978.1:p.Leu160=
XM_011512063.1:c.564T>C (PRKRA)	XP_011510365.1:p.Leu188=
XM_011512064.1:c.564T>C (PRKRA)	XP_011510366.1:p.Leu188=
XM_011512066.1:c.480T>C (PRKRA)	XP_011510368.1:p.Leu160=
XM_011512063.2:c.564T>C (PRKRA)	XP_011510365.1:p.Leu188=
XM_011512066.2:c.480T>C (PRKRA)	XP_011510368.1:p.Leu160=
XM_017005159.1:c.480T>C (PRKRA)	XP_016860648.1:p.Leu160=
XR_001739008.2:n.860T>C (PRKRA)
NM_003690.5:c.819T>C (PRKRA) MANE Select	NP_003681.1:p.Leu273=
NM_001316362.2:c.480T>C (PRKRA)	NP_001303291.1:p.Leu160=