Canonical Allele Identifier: CA349399066

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296933G>C (hg19) ; chr2:g.178432206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432206G>C , CM000664.2:g.178432206G>C	GRCh38
NC_000002.11:g.179296933G>C , CM000664.1:g.179296933G>C	GRCh37
NC_000002.10:g.179005179G>C	NCBI36
NG_009053.1:g.24026C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.833C>G (PRKRA) MANE Select	ENSP00000318176.4:p.Thr278Ser
ENST00000448279.2:c.*561C>G (PRKRA)	ENSP00000388455.1:n.*561C>G
ENST00000457633.2:c.*337C>G (PRKRA)	ENSP00000408668.2:n.*337C>G
ENST00000474793.6:n.974C>G (PRKRA)
ENST00000676505.1:c.*593C>G (PRKRA)	ENSP00000504163.1:n.*593C>G
ENST00000676586.1:n.2970C>G (PRKRA)
ENST00000676752.1:n.2732C>G (PRKRA)
ENST00000676832.1:c.*654C>G (PRKRA)	ENSP00000503231.1:n.*654C>G
ENST00000676922.1:c.*561C>G (PRKRA)	ENSP00000503369.1:n.*561C>G
ENST00000677136.1:n.2825C>G (PRKRA)
ENST00000677206.1:c.*625C>G (PRKRA)	ENSP00000503034.1:n.*625C>G
ENST00000677253.1:c.*530C>G (PRKRA)	ENSP00000503466.1:n.*530C>G
ENST00000677386.1:c.*276C>G (PRKRA)	ENSP00000503003.1:n.*276C>G
ENST00000677460.1:c.*162C>G (PRKRA)	ENSP00000504507.1:n.*162C>G
ENST00000677584.1:c.*671C>G (PRKRA)	ENSP00000504411.1:n.*671C>G
ENST00000677689.1:c.578C>G (PRKRA)	ENSP00000502919.1:p.Thr193Ser
ENST00000677859.1:c.686C>G (PRKRA)
ENST00000677981.1:c.581C>G (PRKRA)	ENSP00000503536.1:p.Thr194Ser
ENST00000678053.1:c.*593C>G (PRKRA)	ENSP00000504330.1:n.*593C>G
ENST00000678058.1:c.577C>G (PRKRA)	ENSP00000503203.1:n.577C>G
ENST00000678167.1:c.*387C>G (PRKRA)	ENSP00000504479.1:n.*387C>G
ENST00000678775.1:c.494C>G (PRKRA)	ENSP00000504030.1:p.Thr165Ser
ENST00000678845.1:c.494C>G (PRKRA)	ENSP00000503011.1:p.Thr165Ser
ENST00000679037.1:c.*501C>G (PRKRA)	ENSP00000504421.1:n.*501C>G
ENST00000679202.1:n.1920C>G (PRKRA)
ENST00000325748.8:c.833C>G (PRKRA)	ENSP00000318176.4:p.Thr278Ser
ENST00000424699.5:c.*625C>G (PRKRA)	ENSP00000408029.1:n.*625C>G
ENST00000432031.6:c.800C>G (PRKRA)	ENSP00000393883.2:p.Thr267Ser
ENST00000487082.5:c.758C>G (PRKRA)	ENSP00000430604.1:p.Thr253Ser
ENST00000490501.5:n.1060C>G (PRKRA)
NM_001139517.1:c.800C>G (PRKRA)	NP_001132989.1:p.Thr267Ser
NM_001139518.1:c.758C>G (PRKRA)	NP_001132990.1:p.Thr253Ser
NM_001316362.1:c.494C>G (PRKRA)	NP_001303291.1:p.Thr165Ser
NM_003690.4:c.833C>G (PRKRA)	NP_003681.1:p.Thr278Ser
NR_110204.1:n.872-1176G>C (CHROMR)
NR_110205.1:n.716-1176G>C (CHROMR)
NR_110206.1:n.651-1176G>C (CHROMR)
XM_005246921.3:c.494C>G (PRKRA)	XP_005246978.1:p.Thr165Ser
XM_011512063.1:c.578C>G (PRKRA)	XP_011510365.1:p.Thr193Ser
XM_011512064.1:c.578C>G (PRKRA)	XP_011510366.1:p.Thr193Ser
XM_011512066.1:c.494C>G (PRKRA)	XP_011510368.1:p.Thr165Ser
XM_011512063.2:c.578C>G (PRKRA)	XP_011510365.1:p.Thr193Ser
XM_011512066.2:c.494C>G (PRKRA)	XP_011510368.1:p.Thr165Ser
XM_017005159.1:c.494C>G (PRKRA)	XP_016860648.1:p.Thr165Ser
XR_001739008.2:n.874C>G (PRKRA)
NM_003690.5:c.833C>G (PRKRA) MANE Select	NP_003681.1:p.Thr278Ser
NM_001316362.2:c.494C>G (PRKRA)	NP_001303291.1:p.Thr165Ser