Canonical Allele Identifier: CA349400543

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179300905C>T (hg19) ; chr2:g.178436178C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178436178C>T , CM000664.2:g.178436178C>T	GRCh38
NC_000002.11:g.179300905C>T , CM000664.1:g.179300905C>T	GRCh37
NC_000002.10:g.179009151C>T	NCBI36
NG_009053.1:g.20054G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.751G>A (PRKRA) MANE Select	ENSP00000318176.4:p.Glu251Lys
ENST00000448279.2:c.*479G>A (PRKRA)	ENSP00000388455.1:n.*479G>A
ENST00000457633.2:c.*255G>A (PRKRA)	ENSP00000408668.2:n.*255G>A
ENST00000474793.6:n.892G>A (PRKRA)
ENST00000676505.1:c.*511G>A (PRKRA)	ENSP00000504163.1:n.*511G>A
ENST00000676586.1:n.2888G>A (PRKRA)
ENST00000676752.1:n.2650G>A (PRKRA)
ENST00000676832.1:c.*572G>A (PRKRA)	ENSP00000503231.1:n.*572G>A
ENST00000676922.1:c.*479G>A (PRKRA)	ENSP00000503369.1:n.*479G>A
ENST00000677136.1:n.2743G>A (PRKRA)
ENST00000677206.1:c.*543G>A (PRKRA)	ENSP00000503034.1:n.*543G>A
ENST00000677253.1:c.*448G>A (PRKRA)	ENSP00000503466.1:n.*448G>A
ENST00000677386.1:c.*194G>A (PRKRA)	ENSP00000503003.1:n.*194G>A
ENST00000677460.1:c.*80G>A (PRKRA)	ENSP00000504507.1:n.*80G>A
ENST00000677584.1:c.*589G>A (PRKRA)	ENSP00000504411.1:n.*589G>A
ENST00000677689.1:c.496G>A (PRKRA)	ENSP00000502919.1:p.Glu166Lys
ENST00000677859.1:c.604G>A (PRKRA)
ENST00000677981.1:c.499G>A (PRKRA)	ENSP00000503536.1:p.Glu167Lys
ENST00000678053.1:c.*511G>A (PRKRA)	ENSP00000504330.1:n.*511G>A
ENST00000678058.1:c.495G>A (PRKRA)	ENSP00000503203.1:n.495G>A
ENST00000678167.1:c.*305G>A (PRKRA)	ENSP00000504479.1:n.*305G>A
ENST00000678775.1:c.412G>A (PRKRA)	ENSP00000504030.1:p.Glu138Lys
ENST00000678845.1:c.412G>A (PRKRA)	ENSP00000503011.1:p.Glu138Lys
ENST00000679037.1:c.*419G>A (PRKRA)	ENSP00000504421.1:n.*419G>A
ENST00000679202.1:n.1838G>A (PRKRA)
ENST00000325748.8:c.751G>A (PRKRA)	ENSP00000318176.4:p.Glu251Lys
ENST00000424699.5:c.*543G>A (PRKRA)	ENSP00000408029.1:n.*543G>A
ENST00000432031.6:c.718G>A (PRKRA)	ENSP00000393883.2:p.Glu240Lys
ENST00000487082.5:c.676G>A (PRKRA)	ENSP00000430604.1:p.Glu226Lys
ENST00000490501.5:n.978G>A (PRKRA)
NM_001139517.1:c.718G>A (PRKRA)	NP_001132989.1:p.Glu240Lys
NM_001139518.1:c.676G>A (PRKRA)	NP_001132990.1:p.Glu226Lys
NM_001316362.1:c.412G>A (PRKRA)	NP_001303291.1:p.Glu138Lys
NM_003690.4:c.751G>A (PRKRA)	NP_003681.1:p.Glu251Lys
NR_110204.1:n.966-2689C>T (CHROMR)
XM_005246921.3:c.412G>A (PRKRA)	XP_005246978.1:p.Glu138Lys
XM_011512063.1:c.496G>A (PRKRA)	XP_011510365.1:p.Glu166Lys
XM_011512064.1:c.496G>A (PRKRA)	XP_011510366.1:p.Glu166Lys
XM_011512066.1:c.412G>A (PRKRA)	XP_011510368.1:p.Glu138Lys
XM_011512063.2:c.496G>A (PRKRA)	XP_011510365.1:p.Glu166Lys
XM_011512066.2:c.412G>A (PRKRA)	XP_011510368.1:p.Glu138Lys
XM_017005159.1:c.412G>A (PRKRA)	XP_016860648.1:p.Glu138Lys
XR_001739008.2:n.792G>A (PRKRA)
NM_003690.5:c.751G>A (PRKRA) MANE Select	NP_003681.1:p.Glu251Lys
NM_001316362.2:c.412G>A (PRKRA)	NP_001303291.1:p.Glu138Lys