Canonical Allele Identifier: CA349400690

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179300940G>A (hg19) ; chr2:g.178436213G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178436213G>A , CM000664.2:g.178436213G>A	GRCh38
NC_000002.11:g.179300940G>A , CM000664.1:g.179300940G>A	GRCh37
NC_000002.10:g.179009186G>A	NCBI36
NG_009053.1:g.20019C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.716C>T (PRKRA) MANE Select	ENSP00000318176.4:p.Thr239Ile
ENST00000448279.2:c.*444C>T (PRKRA)	ENSP00000388455.1:n.*444C>T
ENST00000457633.2:c.*220C>T (PRKRA)	ENSP00000408668.2:n.*220C>T
ENST00000474793.6:n.857C>T (PRKRA)
ENST00000676505.1:c.*476C>T (PRKRA)	ENSP00000504163.1:n.*476C>T
ENST00000676586.1:n.2853C>T (PRKRA)
ENST00000676752.1:n.2615C>T (PRKRA)
ENST00000676832.1:c.*537C>T (PRKRA)	ENSP00000503231.1:n.*537C>T
ENST00000676922.1:c.*444C>T (PRKRA)	ENSP00000503369.1:n.*444C>T
ENST00000677136.1:n.2708C>T (PRKRA)
ENST00000677206.1:c.*508C>T (PRKRA)	ENSP00000503034.1:n.*508C>T
ENST00000677253.1:c.*413C>T (PRKRA)	ENSP00000503466.1:n.*413C>T
ENST00000677386.1:c.*159C>T (PRKRA)	ENSP00000503003.1:n.*159C>T
ENST00000677460.1:c.*45C>T (PRKRA)	ENSP00000504507.1:n.*45C>T
ENST00000677584.1:c.*554C>T (PRKRA)	ENSP00000504411.1:n.*554C>T
ENST00000677689.1:c.461C>T (PRKRA)	ENSP00000502919.1:p.Thr154Ile
ENST00000677859.1:c.569C>T (PRKRA)
ENST00000677981.1:c.464C>T (PRKRA)	ENSP00000503536.1:p.Thr155Ile
ENST00000678053.1:c.*476C>T (PRKRA)	ENSP00000504330.1:n.*476C>T
ENST00000678058.1:c.460C>T (PRKRA)	ENSP00000503203.1:n.460C>T
ENST00000678167.1:c.*270C>T (PRKRA)	ENSP00000504479.1:n.*270C>T
ENST00000678775.1:c.377C>T (PRKRA)	ENSP00000504030.1:p.Thr126Ile
ENST00000678845.1:c.377C>T (PRKRA)	ENSP00000503011.1:p.Thr126Ile
ENST00000679037.1:c.*384C>T (PRKRA)	ENSP00000504421.1:n.*384C>T
ENST00000679202.1:n.1803C>T (PRKRA)
ENST00000325748.8:c.716C>T (PRKRA)	ENSP00000318176.4:p.Thr239Ile
ENST00000424699.5:c.*508C>T (PRKRA)	ENSP00000408029.1:n.*508C>T
ENST00000432031.6:c.683C>T (PRKRA)	ENSP00000393883.2:p.Thr228Ile
ENST00000487082.5:c.641C>T (PRKRA)	ENSP00000430604.1:p.Thr214Ile
ENST00000490501.5:n.943C>T (PRKRA)
NM_001139517.1:c.683C>T (PRKRA)	NP_001132989.1:p.Thr228Ile
NM_001139518.1:c.641C>T (PRKRA)	NP_001132990.1:p.Thr214Ile
NM_001316362.1:c.377C>T (PRKRA)	NP_001303291.1:p.Thr126Ile
NM_003690.4:c.716C>T (PRKRA)	NP_003681.1:p.Thr239Ile
NR_110204.1:n.966-2654G>A (CHROMR)
XM_005246921.3:c.377C>T (PRKRA)	XP_005246978.1:p.Thr126Ile
XM_011512063.1:c.461C>T (PRKRA)	XP_011510365.1:p.Thr154Ile
XM_011512064.1:c.461C>T (PRKRA)	XP_011510366.1:p.Thr154Ile
XM_011512066.1:c.377C>T (PRKRA)	XP_011510368.1:p.Thr126Ile
XM_011512063.2:c.461C>T (PRKRA)	XP_011510365.1:p.Thr154Ile
XM_011512066.2:c.377C>T (PRKRA)	XP_011510368.1:p.Thr126Ile
XM_017005159.1:c.377C>T (PRKRA)	XP_016860648.1:p.Thr126Ile
XR_001739008.2:n.757C>T (PRKRA)
NM_003690.5:c.716C>T (PRKRA) MANE Select	NP_003681.1:p.Thr239Ile
NM_001316362.2:c.377C>T (PRKRA)	NP_001303291.1:p.Thr126Ile