Canonical Allele Identifier: CA349399277

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296955G>T (hg19) ; chr2:g.178432228G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432228G>T , CM000664.2:g.178432228G>T	GRCh38
NC_000002.11:g.179296955G>T , CM000664.1:g.179296955G>T	GRCh37
NC_000002.10:g.179005201G>T	NCBI36
NG_009053.1:g.24004C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.811C>A (PRKRA) MANE Select	ENSP00000318176.4:p.Gln271Lys
ENST00000448279.2:c.*539C>A (PRKRA)	ENSP00000388455.1:n.*539C>A
ENST00000457633.2:c.*315C>A (PRKRA)	ENSP00000408668.2:n.*315C>A
ENST00000474793.6:n.952C>A (PRKRA)
ENST00000676505.1:c.*571C>A (PRKRA)	ENSP00000504163.1:n.*571C>A
ENST00000676586.1:n.2948C>A (PRKRA)
ENST00000676752.1:n.2710C>A (PRKRA)
ENST00000676832.1:c.*632C>A (PRKRA)	ENSP00000503231.1:n.*632C>A
ENST00000676922.1:c.*539C>A (PRKRA)	ENSP00000503369.1:n.*539C>A
ENST00000677136.1:n.2803C>A (PRKRA)
ENST00000677206.1:c.*603C>A (PRKRA)	ENSP00000503034.1:n.*603C>A
ENST00000677253.1:c.*508C>A (PRKRA)	ENSP00000503466.1:n.*508C>A
ENST00000677386.1:c.*254C>A (PRKRA)	ENSP00000503003.1:n.*254C>A
ENST00000677460.1:c.*140C>A (PRKRA)	ENSP00000504507.1:n.*140C>A
ENST00000677584.1:c.*649C>A (PRKRA)	ENSP00000504411.1:n.*649C>A
ENST00000677689.1:c.556C>A (PRKRA)	ENSP00000502919.1:p.Gln186Lys
ENST00000677859.1:c.664C>A (PRKRA)
ENST00000677981.1:c.559C>A (PRKRA)	ENSP00000503536.1:p.Gln187Lys
ENST00000678053.1:c.*571C>A (PRKRA)	ENSP00000504330.1:n.*571C>A
ENST00000678058.1:c.555C>A (PRKRA)	ENSP00000503203.1:n.555C>A
ENST00000678167.1:c.*365C>A (PRKRA)	ENSP00000504479.1:n.*365C>A
ENST00000678775.1:c.472C>A (PRKRA)	ENSP00000504030.1:p.Gln158Lys
ENST00000678845.1:c.472C>A (PRKRA)	ENSP00000503011.1:p.Gln158Lys
ENST00000679037.1:c.*479C>A (PRKRA)	ENSP00000504421.1:n.*479C>A
ENST00000679202.1:n.1898C>A (PRKRA)
ENST00000325748.8:c.811C>A (PRKRA)	ENSP00000318176.4:p.Gln271Lys
ENST00000424699.5:c.*603C>A (PRKRA)	ENSP00000408029.1:n.*603C>A
ENST00000432031.6:c.778C>A (PRKRA)	ENSP00000393883.2:p.Gln260Lys
ENST00000487082.5:c.736C>A (PRKRA)	ENSP00000430604.1:p.Gln246Lys
ENST00000490501.5:n.1038C>A (PRKRA)
NM_001139517.1:c.778C>A (PRKRA)	NP_001132989.1:p.Gln260Lys
NM_001139518.1:c.736C>A (PRKRA)	NP_001132990.1:p.Gln246Lys
NM_001316362.1:c.472C>A (PRKRA)	NP_001303291.1:p.Gln158Lys
NM_003690.4:c.811C>A (PRKRA)	NP_003681.1:p.Gln271Lys
NR_110204.1:n.872-1154G>T (CHROMR)
NR_110205.1:n.716-1154G>T (CHROMR)
NR_110206.1:n.651-1154G>T (CHROMR)
XM_005246921.3:c.472C>A (PRKRA)	XP_005246978.1:p.Gln158Lys
XM_011512063.1:c.556C>A (PRKRA)	XP_011510365.1:p.Gln186Lys
XM_011512064.1:c.556C>A (PRKRA)	XP_011510366.1:p.Gln186Lys
XM_011512066.1:c.472C>A (PRKRA)	XP_011510368.1:p.Gln158Lys
XM_011512063.2:c.556C>A (PRKRA)	XP_011510365.1:p.Gln186Lys
XM_011512066.2:c.472C>A (PRKRA)	XP_011510368.1:p.Gln158Lys
XM_017005159.1:c.472C>A (PRKRA)	XP_016860648.1:p.Gln158Lys
XR_001739008.2:n.852C>A (PRKRA)
NM_003690.5:c.811C>A (PRKRA) MANE Select	NP_003681.1:p.Gln271Lys
NM_001316362.2:c.472C>A (PRKRA)	NP_001303291.1:p.Gln158Lys