Canonical Allele Identifier: CA60962918

Gene: PRKRA CHROMR

Linked Data

• dbSNP Id: rs1037080897
• MyVariant Identifiers: chr2:g.179296964C>T (hg19) ; chr2:g.178432237C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432237C>T , CM000664.2:g.178432237C>T	GRCh38
NC_000002.11:g.179296964C>T , CM000664.1:g.179296964C>T	GRCh37
NC_000002.10:g.179005210C>T	NCBI36
NG_009053.1:g.23995G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.802G>A (PRKRA) MANE Select	ENSP00000318176.4:p.Gly268Arg
ENST00000448279.2:c.*530G>A (PRKRA)	ENSP00000388455.1:n.*530G>A
ENST00000457633.2:c.*306G>A (PRKRA)	ENSP00000408668.2:n.*306G>A
ENST00000474793.6:n.943G>A (PRKRA)
ENST00000676505.1:c.*562G>A (PRKRA)	ENSP00000504163.1:n.*562G>A
ENST00000676586.1:n.2939G>A (PRKRA)
ENST00000676752.1:n.2701G>A (PRKRA)
ENST00000676832.1:c.*623G>A (PRKRA)	ENSP00000503231.1:n.*623G>A
ENST00000676922.1:c.*530G>A (PRKRA)	ENSP00000503369.1:n.*530G>A
ENST00000677136.1:n.2794G>A (PRKRA)
ENST00000677206.1:c.*594G>A (PRKRA)	ENSP00000503034.1:n.*594G>A
ENST00000677253.1:c.*499G>A (PRKRA)	ENSP00000503466.1:n.*499G>A
ENST00000677386.1:c.*245G>A (PRKRA)	ENSP00000503003.1:n.*245G>A
ENST00000677460.1:c.*131G>A (PRKRA)	ENSP00000504507.1:n.*131G>A
ENST00000677584.1:c.*640G>A (PRKRA)	ENSP00000504411.1:n.*640G>A
ENST00000677689.1:c.547G>A (PRKRA)	ENSP00000502919.1:p.Gly183Arg
ENST00000677859.1:c.655G>A (PRKRA)
ENST00000677981.1:c.550G>A (PRKRA)	ENSP00000503536.1:p.Gly184Arg
ENST00000678053.1:c.*562G>A (PRKRA)	ENSP00000504330.1:n.*562G>A
ENST00000678058.1:c.546G>A (PRKRA)	ENSP00000503203.1:n.546G>A
ENST00000678167.1:c.*356G>A (PRKRA)	ENSP00000504479.1:n.*356G>A
ENST00000678775.1:c.463G>A (PRKRA)	ENSP00000504030.1:p.Gly155Arg
ENST00000678845.1:c.463G>A (PRKRA)	ENSP00000503011.1:p.Gly155Arg
ENST00000679037.1:c.*470G>A (PRKRA)	ENSP00000504421.1:n.*470G>A
ENST00000679202.1:n.1889G>A (PRKRA)
ENST00000325748.8:c.802G>A (PRKRA)	ENSP00000318176.4:p.Gly268Arg
ENST00000424699.5:c.*594G>A (PRKRA)	ENSP00000408029.1:n.*594G>A
ENST00000432031.6:c.769G>A (PRKRA)	ENSP00000393883.2:p.Gly257Arg
ENST00000487082.5:c.727G>A (PRKRA)	ENSP00000430604.1:p.Gly243Arg
ENST00000490501.5:n.1029G>A (PRKRA)
NM_001139517.1:c.769G>A (PRKRA)	NP_001132989.1:p.Gly257Arg
NM_001139518.1:c.727G>A (PRKRA)	NP_001132990.1:p.Gly243Arg
NM_001316362.1:c.463G>A (PRKRA)	NP_001303291.1:p.Gly155Arg
NM_003690.4:c.802G>A (PRKRA)	NP_003681.1:p.Gly268Arg
NR_110204.1:n.872-1145C>T (CHROMR)
NR_110205.1:n.716-1145C>T (CHROMR)
NR_110206.1:n.651-1145C>T (CHROMR)
XM_005246921.3:c.463G>A (PRKRA)	XP_005246978.1:p.Gly155Arg
XM_011512063.1:c.547G>A (PRKRA)	XP_011510365.1:p.Gly183Arg
XM_011512064.1:c.547G>A (PRKRA)	XP_011510366.1:p.Gly183Arg
XM_011512066.1:c.463G>A (PRKRA)	XP_011510368.1:p.Gly155Arg
XM_011512063.2:c.547G>A (PRKRA)	XP_011510365.1:p.Gly183Arg
XM_011512066.2:c.463G>A (PRKRA)	XP_011510368.1:p.Gly155Arg
XM_017005159.1:c.463G>A (PRKRA)	XP_016860648.1:p.Gly155Arg
XR_001739008.2:n.843G>A (PRKRA)
NM_003690.5:c.802G>A (PRKRA) MANE Select	NP_003681.1:p.Gly268Arg
NM_001316362.2:c.463G>A (PRKRA)	NP_001303291.1:p.Gly155Arg