Canonical Allele Identifier: CA349399206

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296949G>T (hg19) ; chr2:g.178432222G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432222G>T , CM000664.2:g.178432222G>T	GRCh38
NC_000002.11:g.179296949G>T , CM000664.1:g.179296949G>T	GRCh37
NC_000002.10:g.179005195G>T	NCBI36
NG_009053.1:g.24010C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.817C>A (PRKRA) MANE Select	ENSP00000318176.4:p.Leu273Ile
ENST00000448279.2:c.*545C>A (PRKRA)	ENSP00000388455.1:n.*545C>A
ENST00000457633.2:c.*321C>A (PRKRA)	ENSP00000408668.2:n.*321C>A
ENST00000474793.6:n.958C>A (PRKRA)
ENST00000676505.1:c.*577C>A (PRKRA)	ENSP00000504163.1:n.*577C>A
ENST00000676586.1:n.2954C>A (PRKRA)
ENST00000676752.1:n.2716C>A (PRKRA)
ENST00000676832.1:c.*638C>A (PRKRA)	ENSP00000503231.1:n.*638C>A
ENST00000676922.1:c.*545C>A (PRKRA)	ENSP00000503369.1:n.*545C>A
ENST00000677136.1:n.2809C>A (PRKRA)
ENST00000677206.1:c.*609C>A (PRKRA)	ENSP00000503034.1:n.*609C>A
ENST00000677253.1:c.*514C>A (PRKRA)	ENSP00000503466.1:n.*514C>A
ENST00000677386.1:c.*260C>A (PRKRA)	ENSP00000503003.1:n.*260C>A
ENST00000677460.1:c.*146C>A (PRKRA)	ENSP00000504507.1:n.*146C>A
ENST00000677584.1:c.*655C>A (PRKRA)	ENSP00000504411.1:n.*655C>A
ENST00000677689.1:c.562C>A (PRKRA)	ENSP00000502919.1:p.Leu188Ile
ENST00000677859.1:c.670C>A (PRKRA)
ENST00000677981.1:c.565C>A (PRKRA)	ENSP00000503536.1:p.Leu189Ile
ENST00000678053.1:c.*577C>A (PRKRA)	ENSP00000504330.1:n.*577C>A
ENST00000678058.1:c.561C>A (PRKRA)	ENSP00000503203.1:n.561C>A
ENST00000678167.1:c.*371C>A (PRKRA)	ENSP00000504479.1:n.*371C>A
ENST00000678775.1:c.478C>A (PRKRA)	ENSP00000504030.1:p.Leu160Ile
ENST00000678845.1:c.478C>A (PRKRA)	ENSP00000503011.1:p.Leu160Ile
ENST00000679037.1:c.*485C>A (PRKRA)	ENSP00000504421.1:n.*485C>A
ENST00000679202.1:n.1904C>A (PRKRA)
ENST00000325748.8:c.817C>A (PRKRA)	ENSP00000318176.4:p.Leu273Ile
ENST00000424699.5:c.*609C>A (PRKRA)	ENSP00000408029.1:n.*609C>A
ENST00000432031.6:c.784C>A (PRKRA)	ENSP00000393883.2:p.Leu262Ile
ENST00000487082.5:c.742C>A (PRKRA)	ENSP00000430604.1:p.Leu248Ile
ENST00000490501.5:n.1044C>A (PRKRA)
NM_001139517.1:c.784C>A (PRKRA)	NP_001132989.1:p.Leu262Ile
NM_001139518.1:c.742C>A (PRKRA)	NP_001132990.1:p.Leu248Ile
NM_001316362.1:c.478C>A (PRKRA)	NP_001303291.1:p.Leu160Ile
NM_003690.4:c.817C>A (PRKRA)	NP_003681.1:p.Leu273Ile
NR_110204.1:n.872-1160G>T (CHROMR)
NR_110205.1:n.716-1160G>T (CHROMR)
NR_110206.1:n.651-1160G>T (CHROMR)
XM_005246921.3:c.478C>A (PRKRA)	XP_005246978.1:p.Leu160Ile
XM_011512063.1:c.562C>A (PRKRA)	XP_011510365.1:p.Leu188Ile
XM_011512064.1:c.562C>A (PRKRA)	XP_011510366.1:p.Leu188Ile
XM_011512066.1:c.478C>A (PRKRA)	XP_011510368.1:p.Leu160Ile
XM_011512063.2:c.562C>A (PRKRA)	XP_011510365.1:p.Leu188Ile
XM_011512066.2:c.478C>A (PRKRA)	XP_011510368.1:p.Leu160Ile
XM_017005159.1:c.478C>A (PRKRA)	XP_016860648.1:p.Leu160Ile
XR_001739008.2:n.858C>A (PRKRA)
NM_003690.5:c.817C>A (PRKRA) MANE Select	NP_003681.1:p.Leu273Ile
NM_001316362.2:c.478C>A (PRKRA)	NP_001303291.1:p.Leu160Ile