Canonical Allele Identifier: CA430089896

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296980A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432253A>G , CM000664.2:g.178432253A>G	GRCh38
NC_000002.11:g.179296980A>G , CM000664.1:g.179296980A>G	GRCh37
NC_000002.10:g.179005226A>G	NCBI36
NG_009053.1:g.23979T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.786T>C (PRKRA) MANE Select	ENSP00000318176.4:p.Asp262=
ENST00000448279.2:c.*514T>C (PRKRA)	ENSP00000388455.1:n.*514T>C
ENST00000457633.2:c.*290T>C (PRKRA)	ENSP00000408668.2:n.*290T>C
ENST00000474793.6:n.927T>C (PRKRA)
ENST00000676505.1:c.*546T>C (PRKRA)	ENSP00000504163.1:n.*546T>C
ENST00000676586.1:n.2923T>C (PRKRA)
ENST00000676752.1:n.2685T>C (PRKRA)
ENST00000676832.1:c.*607T>C (PRKRA)	ENSP00000503231.1:n.*607T>C
ENST00000676922.1:c.*514T>C (PRKRA)	ENSP00000503369.1:n.*514T>C
ENST00000677136.1:n.2778T>C (PRKRA)
ENST00000677206.1:c.*578T>C (PRKRA)	ENSP00000503034.1:n.*578T>C
ENST00000677253.1:c.*483T>C (PRKRA)	ENSP00000503466.1:n.*483T>C
ENST00000677386.1:c.*229T>C (PRKRA)	ENSP00000503003.1:n.*229T>C
ENST00000677460.1:c.*115T>C (PRKRA)	ENSP00000504507.1:n.*115T>C
ENST00000677584.1:c.*624T>C (PRKRA)	ENSP00000504411.1:n.*624T>C
ENST00000677689.1:c.531T>C (PRKRA)	ENSP00000502919.1:p.Asp177=
ENST00000677859.1:c.639T>C (PRKRA)
ENST00000677981.1:c.534T>C (PRKRA)	ENSP00000503536.1:p.Asp178=
ENST00000678053.1:c.*546T>C (PRKRA)	ENSP00000504330.1:n.*546T>C
ENST00000678058.1:c.530T>C (PRKRA)	ENSP00000503203.1:n.530T>C
ENST00000678167.1:c.*340T>C (PRKRA)	ENSP00000504479.1:n.*340T>C
ENST00000678775.1:c.447T>C (PRKRA)	ENSP00000504030.1:p.Asp149=
ENST00000678845.1:c.447T>C (PRKRA)	ENSP00000503011.1:p.Asp149=
ENST00000679037.1:c.*454T>C (PRKRA)	ENSP00000504421.1:n.*454T>C
ENST00000679202.1:n.1873T>C (PRKRA)
ENST00000325748.8:c.786T>C (PRKRA)	ENSP00000318176.4:p.Asp262=
ENST00000424699.5:c.*578T>C (PRKRA)	ENSP00000408029.1:n.*578T>C
ENST00000432031.6:c.753T>C (PRKRA)	ENSP00000393883.2:p.Asp251=
ENST00000487082.5:c.711T>C (PRKRA)	ENSP00000430604.1:p.Asp237=
ENST00000490501.5:n.1013T>C (PRKRA)
NM_001139517.1:c.753T>C (PRKRA)	NP_001132989.1:p.Asp251=
NM_001139518.1:c.711T>C (PRKRA)	NP_001132990.1:p.Asp237=
NM_001316362.1:c.447T>C (PRKRA)	NP_001303291.1:p.Asp149=
NM_003690.4:c.786T>C (PRKRA)	NP_003681.1:p.Asp262=
NR_110204.1:n.872-1129A>G (CHROMR)
NR_110205.1:n.716-1129A>G (CHROMR)
NR_110206.1:n.651-1129A>G (CHROMR)
XM_005246921.3:c.447T>C (PRKRA)	XP_005246978.1:p.Asp149=
XM_011512063.1:c.531T>C (PRKRA)	XP_011510365.1:p.Asp177=
XM_011512064.1:c.531T>C (PRKRA)	XP_011510366.1:p.Asp177=
XM_011512066.1:c.447T>C (PRKRA)	XP_011510368.1:p.Asp149=
XM_011512063.2:c.531T>C (PRKRA)	XP_011510365.1:p.Asp177=
XM_011512066.2:c.447T>C (PRKRA)	XP_011510368.1:p.Asp149=
XM_017005159.1:c.447T>C (PRKRA)	XP_016860648.1:p.Asp149=
XR_001739008.2:n.827T>C (PRKRA)
NM_003690.5:c.786T>C (PRKRA) MANE Select	NP_003681.1:p.Asp262=
NM_001316362.2:c.447T>C (PRKRA)	NP_001303291.1:p.Asp149=