Canonical Allele Identifier: CA913089517

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296930_179296941del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432203_178432214del , CM000664.2:g.178432203_178432214del	GRCh38
NC_000002.11:g.179296930_179296941del , CM000664.1:g.179296930_179296941del	GRCh37
NC_000002.10:g.179005176_179005187del	NCBI36
NG_009053.1:g.24018_24029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.825_836del (PRKRA) MANE Select	ENSP00000318176.4:p.Glu275_Ser279delinsAsp
ENST00000448279.2:c.*553_*564del (PRKRA)	ENSP00000388455.1:n.*553_*564del
ENST00000457633.2:c.*329_*340del (PRKRA)	ENSP00000408668.2:n.*329_*340del
ENST00000474793.6:n.966_977del (PRKRA)
ENST00000676505.1:c.*585_*596del (PRKRA)	ENSP00000504163.1:n.*585_*596del
ENST00000676586.1:n.2962_2973del (PRKRA)
ENST00000676752.1:n.2724_2735del (PRKRA)
ENST00000676832.1:c.*646_*657del (PRKRA)	ENSP00000503231.1:n.*646_*657del
ENST00000676922.1:c.*553_*564del (PRKRA)	ENSP00000503369.1:n.*553_*564del
ENST00000677136.1:n.2817_2828del (PRKRA)
ENST00000677206.1:c.*617_*628del (PRKRA)	ENSP00000503034.1:n.*617_*628del
ENST00000677253.1:c.*522_*533del (PRKRA)	ENSP00000503466.1:n.*522_*533del
ENST00000677386.1:c.*268_*279del (PRKRA)	ENSP00000503003.1:n.*268_*279del
ENST00000677460.1:c.*154_*165del (PRKRA)	ENSP00000504507.1:n.*154_*165del
ENST00000677584.1:c.*663_*674del (PRKRA)	ENSP00000504411.1:n.*663_*674del
ENST00000677689.1:c.570_581del (PRKRA)	ENSP00000502919.1:p.Glu190_Ser194delinsAsp
ENST00000677859.1:c.678_689del (PRKRA)
ENST00000677981.1:c.573_584del (PRKRA)	ENSP00000503536.1:p.Glu191_Ser195delinsAsp
ENST00000678053.1:c.*585_*596del (PRKRA)	ENSP00000504330.1:n.*585_*596del
ENST00000678058.1:c.569_580del (PRKRA)	ENSP00000503203.1:n.569_580del
ENST00000678167.1:c.*379_*390del (PRKRA)	ENSP00000504479.1:n.*379_*390del
ENST00000678775.1:c.486_497del (PRKRA)	ENSP00000504030.1:p.Glu162_Ser166delinsAsp
ENST00000678845.1:c.486_497del (PRKRA)	ENSP00000503011.1:p.Glu162_Ser166delinsAsp
ENST00000679037.1:c.*493_*504del (PRKRA)	ENSP00000504421.1:n.*493_*504del
ENST00000679202.1:n.1912_1923del (PRKRA)
ENST00000325748.8:c.825_836del (PRKRA)	ENSP00000318176.4:p.Glu275_Ser279delinsAsp
ENST00000424699.5:c.*617_*628del (PRKRA)	ENSP00000408029.1:n.*617_*628del
ENST00000432031.6:c.792_803del (PRKRA)	ENSP00000393883.2:p.Glu264_Ser268delinsAsp
ENST00000487082.5:c.750_761del (PRKRA)	ENSP00000430604.1:p.Glu250_Ser254delinsAsp
ENST00000490501.5:n.1052_1063del (PRKRA)
NM_001139517.1:c.792_803del (PRKRA)	NP_001132989.1:p.Glu264_Ser268delinsAsp
NM_001139518.1:c.750_761del (PRKRA)	NP_001132990.1:p.Glu250_Ser254delinsAsp
NM_001316362.1:c.486_497del (PRKRA)	NP_001303291.1:p.Glu162_Ser166delinsAsp
NM_003690.4:c.825_836del (PRKRA)	NP_003681.1:p.Glu275_Ser279delinsAsp
NR_110204.1:n.872-1179_872-1168del (CHROMR)
NR_110205.1:n.716-1179_716-1168del (CHROMR)
NR_110206.1:n.651-1179_651-1168del (CHROMR)
XM_005246921.3:c.486_497del (PRKRA)	XP_005246978.1:p.Glu162_Ser166delinsAsp
XM_011512063.1:c.570_581del (PRKRA)	XP_011510365.1:p.Glu190_Ser194delinsAsp
XM_011512064.1:c.570_581del (PRKRA)	XP_011510366.1:p.Glu190_Ser194delinsAsp
XM_011512066.1:c.486_497del (PRKRA)	XP_011510368.1:p.Glu162_Ser166delinsAsp
XM_011512063.2:c.570_581del (PRKRA)	XP_011510365.1:p.Glu190_Ser194delinsAsp
XM_011512066.2:c.486_497del (PRKRA)	XP_011510368.1:p.Glu162_Ser166delinsAsp
XM_017005159.1:c.486_497del (PRKRA)	XP_016860648.1:p.Glu162_Ser166delinsAsp
XR_001739008.2:n.866_877del (PRKRA)
NM_003690.5:c.825_836del (PRKRA) MANE Select	NP_003681.1:p.Glu275_Ser279delinsAsp
NM_001316362.2:c.486_497del (PRKRA)	NP_001303291.1:p.Glu162_Ser166delinsAsp