Canonical Allele Identifier: CA349399214

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296950A>T (hg19) ; chr2:g.178432223A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432223A>T , CM000664.2:g.178432223A>T	GRCh38
NC_000002.11:g.179296950A>T , CM000664.1:g.179296950A>T	GRCh37
NC_000002.10:g.179005196A>T	NCBI36
NG_009053.1:g.24009T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.816T>A (PRKRA) MANE Select	ENSP00000318176.4:p.Cys272Ter
ENST00000448279.2:c.*544T>A (PRKRA)	ENSP00000388455.1:n.*544T>A
ENST00000457633.2:c.*320T>A (PRKRA)	ENSP00000408668.2:n.*320T>A
ENST00000474793.6:n.957T>A (PRKRA)
ENST00000676505.1:c.*576T>A (PRKRA)	ENSP00000504163.1:n.*576T>A
ENST00000676586.1:n.2953T>A (PRKRA)
ENST00000676752.1:n.2715T>A (PRKRA)
ENST00000676832.1:c.*637T>A (PRKRA)	ENSP00000503231.1:n.*637T>A
ENST00000676922.1:c.*544T>A (PRKRA)	ENSP00000503369.1:n.*544T>A
ENST00000677136.1:n.2808T>A (PRKRA)
ENST00000677206.1:c.*608T>A (PRKRA)	ENSP00000503034.1:n.*608T>A
ENST00000677253.1:c.*513T>A (PRKRA)	ENSP00000503466.1:n.*513T>A
ENST00000677386.1:c.*259T>A (PRKRA)	ENSP00000503003.1:n.*259T>A
ENST00000677460.1:c.*145T>A (PRKRA)	ENSP00000504507.1:n.*145T>A
ENST00000677584.1:c.*654T>A (PRKRA)	ENSP00000504411.1:n.*654T>A
ENST00000677689.1:c.561T>A (PRKRA)	ENSP00000502919.1:p.Cys187Ter
ENST00000677859.1:c.669T>A (PRKRA)
ENST00000677981.1:c.564T>A (PRKRA)	ENSP00000503536.1:p.Cys188Ter
ENST00000678053.1:c.*576T>A (PRKRA)	ENSP00000504330.1:n.*576T>A
ENST00000678058.1:c.560T>A (PRKRA)	ENSP00000503203.1:n.560T>A
ENST00000678167.1:c.*370T>A (PRKRA)	ENSP00000504479.1:n.*370T>A
ENST00000678775.1:c.477T>A (PRKRA)	ENSP00000504030.1:p.Cys159Ter
ENST00000678845.1:c.477T>A (PRKRA)	ENSP00000503011.1:p.Cys159Ter
ENST00000679037.1:c.*484T>A (PRKRA)	ENSP00000504421.1:n.*484T>A
ENST00000679202.1:n.1903T>A (PRKRA)
ENST00000325748.8:c.816T>A (PRKRA)	ENSP00000318176.4:p.Cys272Ter
ENST00000424699.5:c.*608T>A (PRKRA)	ENSP00000408029.1:n.*608T>A
ENST00000432031.6:c.783T>A (PRKRA)	ENSP00000393883.2:p.Cys261Ter
ENST00000487082.5:c.741T>A (PRKRA)	ENSP00000430604.1:p.Cys247Ter
ENST00000490501.5:n.1043T>A (PRKRA)
NM_001139517.1:c.783T>A (PRKRA)	NP_001132989.1:p.Cys261Ter
NM_001139518.1:c.741T>A (PRKRA)	NP_001132990.1:p.Cys247Ter
NM_001316362.1:c.477T>A (PRKRA)	NP_001303291.1:p.Cys159Ter
NM_003690.4:c.816T>A (PRKRA)	NP_003681.1:p.Cys272Ter
NR_110204.1:n.872-1159A>T (CHROMR)
NR_110205.1:n.716-1159A>T (CHROMR)
NR_110206.1:n.651-1159A>T (CHROMR)
XM_005246921.3:c.477T>A (PRKRA)	XP_005246978.1:p.Cys159Ter
XM_011512063.1:c.561T>A (PRKRA)	XP_011510365.1:p.Cys187Ter
XM_011512064.1:c.561T>A (PRKRA)	XP_011510366.1:p.Cys187Ter
XM_011512066.1:c.477T>A (PRKRA)	XP_011510368.1:p.Cys159Ter
XM_011512063.2:c.561T>A (PRKRA)	XP_011510365.1:p.Cys187Ter
XM_011512066.2:c.477T>A (PRKRA)	XP_011510368.1:p.Cys159Ter
XM_017005159.1:c.477T>A (PRKRA)	XP_016860648.1:p.Cys159Ter
XR_001739008.2:n.857T>A (PRKRA)
NM_003690.5:c.816T>A (PRKRA) MANE Select	NP_003681.1:p.Cys272Ter
NM_001316362.2:c.477T>A (PRKRA)	NP_001303291.1:p.Cys159Ter