Canonical Allele Identifier: CA430091055

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179300974A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178436247A>G , CM000664.2:g.178436247A>G	GRCh38
NC_000002.11:g.179300974A>G , CM000664.1:g.179300974A>G	GRCh37
NC_000002.10:g.179009220A>G	NCBI36
NG_009053.1:g.19985T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.682T>C (PRKRA) MANE Select	ENSP00000318176.4:p.Leu228=
ENST00000448279.2:c.*410T>C (PRKRA)	ENSP00000388455.1:n.*410T>C
ENST00000457633.2:c.*186T>C (PRKRA)	ENSP00000408668.2:n.*186T>C
ENST00000474793.6:n.823T>C (PRKRA)
ENST00000676505.1:c.*442T>C (PRKRA)	ENSP00000504163.1:n.*442T>C
ENST00000676586.1:n.2819T>C (PRKRA)
ENST00000676752.1:n.2581T>C (PRKRA)
ENST00000676832.1:c.*503T>C (PRKRA)	ENSP00000503231.1:n.*503T>C
ENST00000676922.1:c.*410T>C (PRKRA)	ENSP00000503369.1:n.*410T>C
ENST00000677136.1:n.2674T>C (PRKRA)
ENST00000677206.1:c.*474T>C (PRKRA)	ENSP00000503034.1:n.*474T>C
ENST00000677253.1:c.*379T>C (PRKRA)	ENSP00000503466.1:n.*379T>C
ENST00000677386.1:c.*125T>C (PRKRA)	ENSP00000503003.1:n.*125T>C
ENST00000677460.1:c.*11T>C (PRKRA)	ENSP00000504507.1:n.*11T>C
ENST00000677584.1:c.*520T>C (PRKRA)	ENSP00000504411.1:n.*520T>C
ENST00000677689.1:c.427T>C (PRKRA)	ENSP00000502919.1:p.Leu143=
ENST00000677859.1:c.535T>C (PRKRA)
ENST00000677981.1:c.430T>C (PRKRA)	ENSP00000503536.1:p.Leu144=
ENST00000678053.1:c.*442T>C (PRKRA)	ENSP00000504330.1:n.*442T>C
ENST00000678058.1:c.426T>C (PRKRA)	ENSP00000503203.1:n.426T>C
ENST00000678167.1:c.*236T>C (PRKRA)	ENSP00000504479.1:n.*236T>C
ENST00000678775.1:c.343T>C (PRKRA)	ENSP00000504030.1:p.Leu115=
ENST00000678845.1:c.343T>C (PRKRA)	ENSP00000503011.1:p.Leu115=
ENST00000679037.1:c.*350T>C (PRKRA)	ENSP00000504421.1:n.*350T>C
ENST00000679202.1:n.1769T>C (PRKRA)
ENST00000325748.8:c.682T>C (PRKRA)	ENSP00000318176.4:p.Leu228=
ENST00000424699.5:c.*474T>C (PRKRA)	ENSP00000408029.1:n.*474T>C
ENST00000432031.6:c.649T>C (PRKRA)	ENSP00000393883.2:p.Leu217=
ENST00000487082.5:c.607T>C (PRKRA)	ENSP00000430604.1:p.Leu203=
ENST00000490501.5:n.909T>C (PRKRA)
NM_001139517.1:c.649T>C (PRKRA)	NP_001132989.1:p.Leu217=
NM_001139518.1:c.607T>C (PRKRA)	NP_001132990.1:p.Leu203=
NM_001316362.1:c.343T>C (PRKRA)	NP_001303291.1:p.Leu115=
NM_003690.4:c.682T>C (PRKRA)	NP_003681.1:p.Leu228=
NR_110204.1:n.966-2620A>G (CHROMR)
XM_005246921.3:c.343T>C (PRKRA)	XP_005246978.1:p.Leu115=
XM_011512063.1:c.427T>C (PRKRA)	XP_011510365.1:p.Leu143=
XM_011512064.1:c.427T>C (PRKRA)	XP_011510366.1:p.Leu143=
XM_011512066.1:c.343T>C (PRKRA)	XP_011510368.1:p.Leu115=
XM_011512063.2:c.427T>C (PRKRA)	XP_011510365.1:p.Leu143=
XM_011512066.2:c.343T>C (PRKRA)	XP_011510368.1:p.Leu115=
XM_017005159.1:c.343T>C (PRKRA)	XP_016860648.1:p.Leu115=
XR_001739008.2:n.723T>C (PRKRA)
NM_003690.5:c.682T>C (PRKRA) MANE Select	NP_003681.1:p.Leu228=
NM_001316362.2:c.343T>C (PRKRA)	NP_001303291.1:p.Leu115=