Canonical Allele Identifier: CA60962917

Gene: PRKRA CHROMR

Linked Data

• dbSNP Id: rs36089607

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432237dup , CM000664.2:g.178432237dup	GRCh38
NC_000002.11:g.179296964dup , CM000664.1:g.179296964dup	GRCh37
NC_000002.10:g.179005210dup	NCBI36
NG_009053.1:g.23996dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.803dup (PRKRA) MANE Select	ENSP00000318176.4:p.Gln269ThrfsTer7
ENST00000448279.2:c.*531dup (PRKRA)	ENSP00000388455.1:n.*531dup
ENST00000457633.2:c.*307dup (PRKRA)	ENSP00000408668.2:n.*307dup
ENST00000474793.6:n.944dup (PRKRA)
ENST00000676505.1:c.*563dup (PRKRA)	ENSP00000504163.1:n.*563dup
ENST00000676586.1:n.2940dup (PRKRA)
ENST00000676752.1:n.2702dup (PRKRA)
ENST00000676832.1:c.*624dup (PRKRA)	ENSP00000503231.1:n.*624dup
ENST00000676922.1:c.*531dup (PRKRA)	ENSP00000503369.1:n.*531dup
ENST00000677136.1:n.2795dup (PRKRA)
ENST00000677206.1:c.*595dup (PRKRA)	ENSP00000503034.1:n.*595dup
ENST00000677253.1:c.*500dup (PRKRA)	ENSP00000503466.1:n.*500dup
ENST00000677386.1:c.*246dup (PRKRA)	ENSP00000503003.1:n.*246dup
ENST00000677460.1:c.*132dup (PRKRA)	ENSP00000504507.1:n.*132dup
ENST00000677584.1:c.*641dup (PRKRA)	ENSP00000504411.1:n.*641dup
ENST00000677689.1:c.548dup (PRKRA)	ENSP00000502919.1:p.Gln184ThrfsTer7
ENST00000677859.1:c.656dup (PRKRA)
ENST00000677981.1:c.551dup (PRKRA)	ENSP00000503536.1:p.Gln185ThrfsTer7
ENST00000678053.1:c.*563dup (PRKRA)	ENSP00000504330.1:n.*563dup
ENST00000678058.1:c.547dup (PRKRA)	ENSP00000503203.1:n.547dup
ENST00000678167.1:c.*357dup (PRKRA)	ENSP00000504479.1:n.*357dup
ENST00000678775.1:c.464dup (PRKRA)	ENSP00000504030.1:p.Gln156ThrfsTer7
ENST00000678845.1:c.464dup (PRKRA)	ENSP00000503011.1:p.Gln156ThrfsTer7
ENST00000679037.1:c.*471dup (PRKRA)	ENSP00000504421.1:n.*471dup
ENST00000679202.1:n.1890dup (PRKRA)
ENST00000325748.8:c.803dup (PRKRA)	ENSP00000318176.4:p.Gln269ThrfsTer7
ENST00000424699.5:c.*595dup (PRKRA)	ENSP00000408029.1:n.*595dup
ENST00000432031.6:c.770dup (PRKRA)	ENSP00000393883.2:p.Gln258ThrfsTer7
ENST00000487082.5:c.728dup (PRKRA)	ENSP00000430604.1:p.Gln244ThrfsTer7
ENST00000490501.5:n.1030dup (PRKRA)
NM_001139517.1:c.770dup (PRKRA)	NP_001132989.1:p.Gln258ThrfsTer7
NM_001139518.1:c.728dup (PRKRA)	NP_001132990.1:p.Gln244ThrfsTer7
NM_001316362.1:c.464dup (PRKRA)	NP_001303291.1:p.Gln156ThrfsTer7
NM_003690.4:c.803dup (PRKRA)	NP_003681.1:p.Gln269ThrfsTer7
NR_110204.1:n.872-1145dup (CHROMR)
NR_110205.1:n.716-1145dup (CHROMR)
NR_110206.1:n.651-1145dup (CHROMR)
XM_005246921.3:c.464dup (PRKRA)	XP_005246978.1:p.Gln156ThrfsTer7
XM_011512063.1:c.548dup (PRKRA)	XP_011510365.1:p.Gln184ThrfsTer7
XM_011512064.1:c.548dup (PRKRA)	XP_011510366.1:p.Gln184ThrfsTer7
XM_011512066.1:c.464dup (PRKRA)	XP_011510368.1:p.Gln156ThrfsTer7
XM_011512063.2:c.548dup (PRKRA)	XP_011510365.1:p.Gln184ThrfsTer7
XM_011512066.2:c.464dup (PRKRA)	XP_011510368.1:p.Gln156ThrfsTer7
XM_017005159.1:c.464dup (PRKRA)	XP_016860648.1:p.Gln156ThrfsTer7
XR_001739008.2:n.844dup (PRKRA)
NM_003690.5:c.803dup (PRKRA) MANE Select	NP_003681.1:p.Gln269ThrfsTer7
NM_001316362.2:c.464dup (PRKRA)	NP_001303291.1:p.Gln156ThrfsTer7