Canonical Allele Identifier: CA1310471745

Gene: PRKRA CHROMR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432165C= , CM000664.2:g.178432165C=	GRCh38
NC_000002.11:g.179296892C= , CM000664.1:g.179296892C=	GRCh37
NC_000002.10:g.179005138C=	NCBI36
NG_009053.1:g.24067G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.874G= (PRKRA) MANE Select	ENSP00000318176.4:p.Gly292=
ENST00000448279.2:c.*602G= (PRKRA)	ENSP00000388455.1:n.*602G=
ENST00000457633.2:c.*378G= (PRKRA)	ENSP00000408668.2:n.*378G=
ENST00000474793.6:n.1015G= (PRKRA)
ENST00000676505.1:c.*634G= (PRKRA)	ENSP00000504163.1:n.*634G=
ENST00000676586.1:n.3011G= (PRKRA)
ENST00000676752.1:n.2773G= (PRKRA)
ENST00000676832.1:c.*695G= (PRKRA)	ENSP00000503231.1:n.*695G=
ENST00000676922.1:c.*602G= (PRKRA)	ENSP00000503369.1:n.*602G=
ENST00000677136.1:n.2866G= (PRKRA)
ENST00000677206.1:c.*666G= (PRKRA)	ENSP00000503034.1:n.*666G=
ENST00000677253.1:c.*571G= (PRKRA)	ENSP00000503466.1:n.*571G=
ENST00000677386.1:c.*317G= (PRKRA)	ENSP00000503003.1:n.*317G=
ENST00000677460.1:c.*203G= (PRKRA)	ENSP00000504507.1:n.*203G=
ENST00000677584.1:c.*712G= (PRKRA)	ENSP00000504411.1:n.*712G=
ENST00000677689.1:c.619G= (PRKRA)	ENSP00000502919.1:p.Gly207=
ENST00000677859.1:c.727G= (PRKRA)
ENST00000677981.1:c.622G= (PRKRA)	ENSP00000503536.1:p.Gly208=
ENST00000678053.1:c.*634G= (PRKRA)	ENSP00000504330.1:n.*634G=
ENST00000678058.1:c.618G= (PRKRA)	ENSP00000503203.1:n.618G=
ENST00000678167.1:c.*428G= (PRKRA)	ENSP00000504479.1:n.*428G=
ENST00000678775.1:c.535G= (PRKRA)	ENSP00000504030.1:p.Gly179=
ENST00000678845.1:c.535G= (PRKRA)	ENSP00000503011.1:p.Gly179=
ENST00000679037.1:c.*542G= (PRKRA)	ENSP00000504421.1:n.*542G=
ENST00000679202.1:n.1961G= (PRKRA)
ENST00000325748.8:c.874G= (PRKRA)	ENSP00000318176.4:p.Gly292=
ENST00000424699.5:c.*666G= (PRKRA)	ENSP00000408029.1:n.*666G=
ENST00000432031.6:c.841G= (PRKRA)	ENSP00000393883.2:p.Gly281=
ENST00000487082.5:c.799G= (PRKRA)	ENSP00000430604.1:p.Gly267=
ENST00000490501.5:n.1101G= (PRKRA)
NM_001139517.1:c.841G= (PRKRA)	NP_001132989.1:p.Gly281=
NM_001139518.1:c.799G= (PRKRA)	NP_001132990.1:p.Gly267=
NM_001316362.1:c.535G= (PRKRA)	NP_001303291.1:p.Gly179=
NM_003690.4:c.874G= (PRKRA)	NP_003681.1:p.Gly292=
NR_110204.1:n.872-1217C= (CHROMR)
NR_110205.1:n.716-1217C= (CHROMR)
NR_110206.1:n.651-1217C= (CHROMR)
XM_005246921.3:c.535G= (PRKRA)	XP_005246978.1:p.Gly179=
XM_011512063.1:c.619G= (PRKRA)	XP_011510365.1:p.Gly207=
XM_011512064.1:c.619G= (PRKRA)	XP_011510366.1:p.Gly207=
XM_011512066.1:c.535G= (PRKRA)	XP_011510368.1:p.Gly179=
XM_011512063.2:c.619G= (PRKRA)	XP_011510365.1:p.Gly207=
XM_011512066.2:c.535G= (PRKRA)	XP_011510368.1:p.Gly179=
XM_017005159.1:c.535G= (PRKRA)	XP_016860648.1:p.Gly179=
XR_001739008.2:n.915G= (PRKRA)
NM_003690.5:c.874G= (PRKRA) MANE Select	NP_003681.1:p.Gly292=
NM_001316362.2:c.535G= (PRKRA)	NP_001303291.1:p.Gly179=