Canonical Allele Identifier: CA349398676

Gene: PRKRA CHROMR

Linked Data

• COSMIC: COSM322824
• MyVariant Identifiers: chr2:g.179296885G>C (hg19) ; chr2:g.178432158G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432158G>C , CM000664.2:g.178432158G>C	GRCh38
NC_000002.11:g.179296885G>C , CM000664.1:g.179296885G>C	GRCh37
NC_000002.10:g.179005131G>C	NCBI36
NG_009053.1:g.24074C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.881C>G (PRKRA) MANE Select	ENSP00000318176.4:p.Ala294Gly
ENST00000448279.2:c.*609C>G (PRKRA)	ENSP00000388455.1:n.*609C>G
ENST00000457633.2:c.*385C>G (PRKRA)	ENSP00000408668.2:n.*385C>G
ENST00000474793.6:n.1022C>G (PRKRA)
ENST00000676505.1:c.*641C>G (PRKRA)	ENSP00000504163.1:n.*641C>G
ENST00000676586.1:n.3018C>G (PRKRA)
ENST00000676752.1:n.2780C>G (PRKRA)
ENST00000676832.1:c.*702C>G (PRKRA)	ENSP00000503231.1:n.*702C>G
ENST00000676922.1:c.*609C>G (PRKRA)	ENSP00000503369.1:n.*609C>G
ENST00000677136.1:n.2873C>G (PRKRA)
ENST00000677206.1:c.*673C>G (PRKRA)	ENSP00000503034.1:n.*673C>G
ENST00000677253.1:c.*578C>G (PRKRA)	ENSP00000503466.1:n.*578C>G
ENST00000677386.1:c.*324C>G (PRKRA)	ENSP00000503003.1:n.*324C>G
ENST00000677460.1:c.*210C>G (PRKRA)	ENSP00000504507.1:n.*210C>G
ENST00000677584.1:c.*719C>G (PRKRA)	ENSP00000504411.1:n.*719C>G
ENST00000677689.1:c.626C>G (PRKRA)	ENSP00000502919.1:p.Ala209Gly
ENST00000677859.1:c.734C>G (PRKRA)
ENST00000677981.1:c.629C>G (PRKRA)	ENSP00000503536.1:p.Ala210Gly
ENST00000678053.1:c.*641C>G (PRKRA)	ENSP00000504330.1:n.*641C>G
ENST00000678058.1:c.625C>G (PRKRA)	ENSP00000503203.1:n.625C>G
ENST00000678167.1:c.*435C>G (PRKRA)	ENSP00000504479.1:n.*435C>G
ENST00000678775.1:c.542C>G (PRKRA)	ENSP00000504030.1:p.Ala181Gly
ENST00000678845.1:c.542C>G (PRKRA)	ENSP00000503011.1:p.Ala181Gly
ENST00000679037.1:c.*549C>G (PRKRA)	ENSP00000504421.1:n.*549C>G
ENST00000679202.1:n.1968C>G (PRKRA)
ENST00000325748.8:c.881C>G (PRKRA)	ENSP00000318176.4:p.Ala294Gly
ENST00000424699.5:c.*673C>G (PRKRA)	ENSP00000408029.1:n.*673C>G
ENST00000432031.6:c.848C>G (PRKRA)	ENSP00000393883.2:p.Ala283Gly
ENST00000487082.5:c.806C>G (PRKRA)	ENSP00000430604.1:p.Ala269Gly
ENST00000490501.5:n.1108C>G (PRKRA)
NM_001139517.1:c.848C>G (PRKRA)	NP_001132989.1:p.Ala283Gly
NM_001139518.1:c.806C>G (PRKRA)	NP_001132990.1:p.Ala269Gly
NM_001316362.1:c.542C>G (PRKRA)	NP_001303291.1:p.Ala181Gly
NM_003690.4:c.881C>G (PRKRA)	NP_003681.1:p.Ala294Gly
NR_110204.1:n.872-1224G>C (CHROMR)
NR_110205.1:n.716-1224G>C (CHROMR)
NR_110206.1:n.651-1224G>C (CHROMR)
XM_005246921.3:c.542C>G (PRKRA)	XP_005246978.1:p.Ala181Gly
XM_011512063.1:c.626C>G (PRKRA)	XP_011510365.1:p.Ala209Gly
XM_011512064.1:c.626C>G (PRKRA)	XP_011510366.1:p.Ala209Gly
XM_011512066.1:c.542C>G (PRKRA)	XP_011510368.1:p.Ala181Gly
XM_011512063.2:c.626C>G (PRKRA)	XP_011510365.1:p.Ala209Gly
XM_011512066.2:c.542C>G (PRKRA)	XP_011510368.1:p.Ala181Gly
XM_017005159.1:c.542C>G (PRKRA)	XP_016860648.1:p.Ala181Gly
XR_001739008.2:n.922C>G (PRKRA)
NM_003690.5:c.881C>G (PRKRA) MANE Select	NP_003681.1:p.Ala294Gly
NM_001316362.2:c.542C>G (PRKRA)	NP_001303291.1:p.Ala181Gly