Canonical Allele Identifier: CA349398960

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296922T>A (hg19) ; chr2:g.178432195T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432195T>A , CM000664.2:g.178432195T>A	GRCh38
NC_000002.11:g.179296922T>A , CM000664.1:g.179296922T>A	GRCh37
NC_000002.10:g.179005168T>A	NCBI36
NG_009053.1:g.24037A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.844A>T (PRKRA) MANE Select	ENSP00000318176.4:p.Thr282Ser
ENST00000448279.2:c.*572A>T (PRKRA)	ENSP00000388455.1:n.*572A>T
ENST00000457633.2:c.*348A>T (PRKRA)	ENSP00000408668.2:n.*348A>T
ENST00000474793.6:n.985A>T (PRKRA)
ENST00000676505.1:c.*604A>T (PRKRA)	ENSP00000504163.1:n.*604A>T
ENST00000676586.1:n.2981A>T (PRKRA)
ENST00000676752.1:n.2743A>T (PRKRA)
ENST00000676832.1:c.*665A>T (PRKRA)	ENSP00000503231.1:n.*665A>T
ENST00000676922.1:c.*572A>T (PRKRA)	ENSP00000503369.1:n.*572A>T
ENST00000677136.1:n.2836A>T (PRKRA)
ENST00000677206.1:c.*636A>T (PRKRA)	ENSP00000503034.1:n.*636A>T
ENST00000677253.1:c.*541A>T (PRKRA)	ENSP00000503466.1:n.*541A>T
ENST00000677386.1:c.*287A>T (PRKRA)	ENSP00000503003.1:n.*287A>T
ENST00000677460.1:c.*173A>T (PRKRA)	ENSP00000504507.1:n.*173A>T
ENST00000677584.1:c.*682A>T (PRKRA)	ENSP00000504411.1:n.*682A>T
ENST00000677689.1:c.589A>T (PRKRA)	ENSP00000502919.1:p.Thr197Ser
ENST00000677859.1:c.697A>T (PRKRA)
ENST00000677981.1:c.592A>T (PRKRA)	ENSP00000503536.1:p.Thr198Ser
ENST00000678053.1:c.*604A>T (PRKRA)	ENSP00000504330.1:n.*604A>T
ENST00000678058.1:c.588A>T (PRKRA)	ENSP00000503203.1:n.588A>T
ENST00000678167.1:c.*398A>T (PRKRA)	ENSP00000504479.1:n.*398A>T
ENST00000678775.1:c.505A>T (PRKRA)	ENSP00000504030.1:p.Thr169Ser
ENST00000678845.1:c.505A>T (PRKRA)	ENSP00000503011.1:p.Thr169Ser
ENST00000679037.1:c.*512A>T (PRKRA)	ENSP00000504421.1:n.*512A>T
ENST00000679202.1:n.1931A>T (PRKRA)
ENST00000325748.8:c.844A>T (PRKRA)	ENSP00000318176.4:p.Thr282Ser
ENST00000424699.5:c.*636A>T (PRKRA)	ENSP00000408029.1:n.*636A>T
ENST00000432031.6:c.811A>T (PRKRA)	ENSP00000393883.2:p.Thr271Ser
ENST00000487082.5:c.769A>T (PRKRA)	ENSP00000430604.1:p.Thr257Ser
ENST00000490501.5:n.1071A>T (PRKRA)
NM_001139517.1:c.811A>T (PRKRA)	NP_001132989.1:p.Thr271Ser
NM_001139518.1:c.769A>T (PRKRA)	NP_001132990.1:p.Thr257Ser
NM_001316362.1:c.505A>T (PRKRA)	NP_001303291.1:p.Thr169Ser
NM_003690.4:c.844A>T (PRKRA)	NP_003681.1:p.Thr282Ser
NR_110204.1:n.872-1187T>A (CHROMR)
NR_110205.1:n.716-1187T>A (CHROMR)
NR_110206.1:n.651-1187T>A (CHROMR)
XM_005246921.3:c.505A>T (PRKRA)	XP_005246978.1:p.Thr169Ser
XM_011512063.1:c.589A>T (PRKRA)	XP_011510365.1:p.Thr197Ser
XM_011512064.1:c.589A>T (PRKRA)	XP_011510366.1:p.Thr197Ser
XM_011512066.1:c.505A>T (PRKRA)	XP_011510368.1:p.Thr169Ser
XM_011512063.2:c.589A>T (PRKRA)	XP_011510365.1:p.Thr197Ser
XM_011512066.2:c.505A>T (PRKRA)	XP_011510368.1:p.Thr169Ser
XM_017005159.1:c.505A>T (PRKRA)	XP_016860648.1:p.Thr169Ser
XR_001739008.2:n.885A>T (PRKRA)
NM_003690.5:c.844A>T (PRKRA) MANE Select	NP_003681.1:p.Thr282Ser
NM_001316362.2:c.505A>T (PRKRA)	NP_001303291.1:p.Thr169Ser