Canonical Allele Identifier: CA349398901

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296915C>G (hg19) ; chr2:g.178432188C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432188C>G , CM000664.2:g.178432188C>G	GRCh38
NC_000002.11:g.179296915C>G , CM000664.1:g.179296915C>G	GRCh37
NC_000002.10:g.179005161C>G	NCBI36
NG_009053.1:g.24044G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.851G>C (PRKRA) MANE Select	ENSP00000318176.4:p.Cys284Ser
ENST00000448279.2:c.*579G>C (PRKRA)	ENSP00000388455.1:n.*579G>C
ENST00000457633.2:c.*355G>C (PRKRA)	ENSP00000408668.2:n.*355G>C
ENST00000474793.6:n.992G>C (PRKRA)
ENST00000676505.1:c.*611G>C (PRKRA)	ENSP00000504163.1:n.*611G>C
ENST00000676586.1:n.2988G>C (PRKRA)
ENST00000676752.1:n.2750G>C (PRKRA)
ENST00000676832.1:c.*672G>C (PRKRA)	ENSP00000503231.1:n.*672G>C
ENST00000676922.1:c.*579G>C (PRKRA)	ENSP00000503369.1:n.*579G>C
ENST00000677136.1:n.2843G>C (PRKRA)
ENST00000677206.1:c.*643G>C (PRKRA)	ENSP00000503034.1:n.*643G>C
ENST00000677253.1:c.*548G>C (PRKRA)	ENSP00000503466.1:n.*548G>C
ENST00000677386.1:c.*294G>C (PRKRA)	ENSP00000503003.1:n.*294G>C
ENST00000677460.1:c.*180G>C (PRKRA)	ENSP00000504507.1:n.*180G>C
ENST00000677584.1:c.*689G>C (PRKRA)	ENSP00000504411.1:n.*689G>C
ENST00000677689.1:c.596G>C (PRKRA)	ENSP00000502919.1:p.Cys199Ser
ENST00000677859.1:c.704G>C (PRKRA)
ENST00000677981.1:c.599G>C (PRKRA)	ENSP00000503536.1:p.Cys200Ser
ENST00000678053.1:c.*611G>C (PRKRA)	ENSP00000504330.1:n.*611G>C
ENST00000678058.1:c.595G>C (PRKRA)	ENSP00000503203.1:n.595G>C
ENST00000678167.1:c.*405G>C (PRKRA)	ENSP00000504479.1:n.*405G>C
ENST00000678775.1:c.512G>C (PRKRA)	ENSP00000504030.1:p.Cys171Ser
ENST00000678845.1:c.512G>C (PRKRA)	ENSP00000503011.1:p.Cys171Ser
ENST00000679037.1:c.*519G>C (PRKRA)	ENSP00000504421.1:n.*519G>C
ENST00000679202.1:n.1938G>C (PRKRA)
ENST00000325748.8:c.851G>C (PRKRA)	ENSP00000318176.4:p.Cys284Ser
ENST00000424699.5:c.*643G>C (PRKRA)	ENSP00000408029.1:n.*643G>C
ENST00000432031.6:c.818G>C (PRKRA)	ENSP00000393883.2:p.Cys273Ser
ENST00000487082.5:c.776G>C (PRKRA)	ENSP00000430604.1:p.Cys259Ser
ENST00000490501.5:n.1078G>C (PRKRA)
NM_001139517.1:c.818G>C (PRKRA)	NP_001132989.1:p.Cys273Ser
NM_001139518.1:c.776G>C (PRKRA)	NP_001132990.1:p.Cys259Ser
NM_001316362.1:c.512G>C (PRKRA)	NP_001303291.1:p.Cys171Ser
NM_003690.4:c.851G>C (PRKRA)	NP_003681.1:p.Cys284Ser
NR_110204.1:n.872-1194C>G (CHROMR)
NR_110205.1:n.716-1194C>G (CHROMR)
NR_110206.1:n.651-1194C>G (CHROMR)
XM_005246921.3:c.512G>C (PRKRA)	XP_005246978.1:p.Cys171Ser
XM_011512063.1:c.596G>C (PRKRA)	XP_011510365.1:p.Cys199Ser
XM_011512064.1:c.596G>C (PRKRA)	XP_011510366.1:p.Cys199Ser
XM_011512066.1:c.512G>C (PRKRA)	XP_011510368.1:p.Cys171Ser
XM_011512063.2:c.596G>C (PRKRA)	XP_011510365.1:p.Cys199Ser
XM_011512066.2:c.512G>C (PRKRA)	XP_011510368.1:p.Cys171Ser
XM_017005159.1:c.512G>C (PRKRA)	XP_016860648.1:p.Cys171Ser
XR_001739008.2:n.892G>C (PRKRA)
NM_003690.5:c.851G>C (PRKRA) MANE Select	NP_003681.1:p.Cys284Ser
NM_001316362.2:c.512G>C (PRKRA)	NP_001303291.1:p.Cys171Ser