Canonical Allele Identifier: CA349398924

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296918A>G (hg19) ; chr2:g.178432191A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432191A>G , CM000664.2:g.178432191A>G	GRCh38
NC_000002.11:g.179296918A>G , CM000664.1:g.179296918A>G	GRCh37
NC_000002.10:g.179005164A>G	NCBI36
NG_009053.1:g.24041T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.848T>C (PRKRA) MANE Select	ENSP00000318176.4:p.Val283Ala
ENST00000448279.2:c.*576T>C (PRKRA)	ENSP00000388455.1:n.*576T>C
ENST00000457633.2:c.*352T>C (PRKRA)	ENSP00000408668.2:n.*352T>C
ENST00000474793.6:n.989T>C (PRKRA)
ENST00000676505.1:c.*608T>C (PRKRA)	ENSP00000504163.1:n.*608T>C
ENST00000676586.1:n.2985T>C (PRKRA)
ENST00000676752.1:n.2747T>C (PRKRA)
ENST00000676832.1:c.*669T>C (PRKRA)	ENSP00000503231.1:n.*669T>C
ENST00000676922.1:c.*576T>C (PRKRA)	ENSP00000503369.1:n.*576T>C
ENST00000677136.1:n.2840T>C (PRKRA)
ENST00000677206.1:c.*640T>C (PRKRA)	ENSP00000503034.1:n.*640T>C
ENST00000677253.1:c.*545T>C (PRKRA)	ENSP00000503466.1:n.*545T>C
ENST00000677386.1:c.*291T>C (PRKRA)	ENSP00000503003.1:n.*291T>C
ENST00000677460.1:c.*177T>C (PRKRA)	ENSP00000504507.1:n.*177T>C
ENST00000677584.1:c.*686T>C (PRKRA)	ENSP00000504411.1:n.*686T>C
ENST00000677689.1:c.593T>C (PRKRA)	ENSP00000502919.1:p.Val198Ala
ENST00000677859.1:c.701T>C (PRKRA)
ENST00000677981.1:c.596T>C (PRKRA)	ENSP00000503536.1:p.Val199Ala
ENST00000678053.1:c.*608T>C (PRKRA)	ENSP00000504330.1:n.*608T>C
ENST00000678058.1:c.592T>C (PRKRA)	ENSP00000503203.1:n.592T>C
ENST00000678167.1:c.*402T>C (PRKRA)	ENSP00000504479.1:n.*402T>C
ENST00000678775.1:c.509T>C (PRKRA)	ENSP00000504030.1:p.Val170Ala
ENST00000678845.1:c.509T>C (PRKRA)	ENSP00000503011.1:p.Val170Ala
ENST00000679037.1:c.*516T>C (PRKRA)	ENSP00000504421.1:n.*516T>C
ENST00000679202.1:n.1935T>C (PRKRA)
ENST00000325748.8:c.848T>C (PRKRA)	ENSP00000318176.4:p.Val283Ala
ENST00000424699.5:c.*640T>C (PRKRA)	ENSP00000408029.1:n.*640T>C
ENST00000432031.6:c.815T>C (PRKRA)	ENSP00000393883.2:p.Val272Ala
ENST00000487082.5:c.773T>C (PRKRA)	ENSP00000430604.1:p.Val258Ala
ENST00000490501.5:n.1075T>C (PRKRA)
NM_001139517.1:c.815T>C (PRKRA)	NP_001132989.1:p.Val272Ala
NM_001139518.1:c.773T>C (PRKRA)	NP_001132990.1:p.Val258Ala
NM_001316362.1:c.509T>C (PRKRA)	NP_001303291.1:p.Val170Ala
NM_003690.4:c.848T>C (PRKRA)	NP_003681.1:p.Val283Ala
NR_110204.1:n.872-1191A>G (CHROMR)
NR_110205.1:n.716-1191A>G (CHROMR)
NR_110206.1:n.651-1191A>G (CHROMR)
XM_005246921.3:c.509T>C (PRKRA)	XP_005246978.1:p.Val170Ala
XM_011512063.1:c.593T>C (PRKRA)	XP_011510365.1:p.Val198Ala
XM_011512064.1:c.593T>C (PRKRA)	XP_011510366.1:p.Val198Ala
XM_011512066.1:c.509T>C (PRKRA)	XP_011510368.1:p.Val170Ala
XM_011512063.2:c.593T>C (PRKRA)	XP_011510365.1:p.Val198Ala
XM_011512066.2:c.509T>C (PRKRA)	XP_011510368.1:p.Val170Ala
XM_017005159.1:c.509T>C (PRKRA)	XP_016860648.1:p.Val170Ala
XR_001739008.2:n.889T>C (PRKRA)
NM_003690.5:c.848T>C (PRKRA) MANE Select	NP_003681.1:p.Val283Ala
NM_001316362.2:c.509T>C (PRKRA)	NP_001303291.1:p.Val170Ala