Canonical Allele Identifier: CA430089850

Gene: PRKRA CHROMR

Linked Data

• gnomAD v4: 2-178432181-G-A
• MyVariant Identifiers: chr2:g.179296908G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432181G>A , CM000664.2:g.178432181G>A	GRCh38
NC_000002.11:g.179296908G>A , CM000664.1:g.179296908G>A	GRCh37
NC_000002.10:g.179005154G>A	NCBI36
NG_009053.1:g.24051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.858C>T (PRKRA) MANE Select	ENSP00000318176.4:p.Gly286=
ENST00000448279.2:c.*586C>T (PRKRA)	ENSP00000388455.1:n.*586C>T
ENST00000457633.2:c.*362C>T (PRKRA)	ENSP00000408668.2:n.*362C>T
ENST00000474793.6:n.999C>T (PRKRA)
ENST00000676505.1:c.*618C>T (PRKRA)	ENSP00000504163.1:n.*618C>T
ENST00000676586.1:n.2995C>T (PRKRA)
ENST00000676752.1:n.2757C>T (PRKRA)
ENST00000676832.1:c.*679C>T (PRKRA)	ENSP00000503231.1:n.*679C>T
ENST00000676922.1:c.*586C>T (PRKRA)	ENSP00000503369.1:n.*586C>T
ENST00000677136.1:n.2850C>T (PRKRA)
ENST00000677206.1:c.*650C>T (PRKRA)	ENSP00000503034.1:n.*650C>T
ENST00000677253.1:c.*555C>T (PRKRA)	ENSP00000503466.1:n.*555C>T
ENST00000677386.1:c.*301C>T (PRKRA)	ENSP00000503003.1:n.*301C>T
ENST00000677460.1:c.*187C>T (PRKRA)	ENSP00000504507.1:n.*187C>T
ENST00000677584.1:c.*696C>T (PRKRA)	ENSP00000504411.1:n.*696C>T
ENST00000677689.1:c.603C>T (PRKRA)	ENSP00000502919.1:p.Gly201=
ENST00000677859.1:c.711C>T (PRKRA)
ENST00000677981.1:c.606C>T (PRKRA)	ENSP00000503536.1:p.Gly202=
ENST00000678053.1:c.*618C>T (PRKRA)	ENSP00000504330.1:n.*618C>T
ENST00000678058.1:c.602C>T (PRKRA)	ENSP00000503203.1:n.602C>T
ENST00000678167.1:c.*412C>T (PRKRA)	ENSP00000504479.1:n.*412C>T
ENST00000678775.1:c.519C>T (PRKRA)	ENSP00000504030.1:p.Gly173=
ENST00000678845.1:c.519C>T (PRKRA)	ENSP00000503011.1:p.Gly173=
ENST00000679037.1:c.*526C>T (PRKRA)	ENSP00000504421.1:n.*526C>T
ENST00000679202.1:n.1945C>T (PRKRA)
ENST00000325748.8:c.858C>T (PRKRA)	ENSP00000318176.4:p.Gly286=
ENST00000424699.5:c.*650C>T (PRKRA)	ENSP00000408029.1:n.*650C>T
ENST00000432031.6:c.825C>T (PRKRA)	ENSP00000393883.2:p.Gly275=
ENST00000487082.5:c.783C>T (PRKRA)	ENSP00000430604.1:p.Gly261=
ENST00000490501.5:n.1085C>T (PRKRA)
NM_001139517.1:c.825C>T (PRKRA)	NP_001132989.1:p.Gly275=
NM_001139518.1:c.783C>T (PRKRA)	NP_001132990.1:p.Gly261=
NM_001316362.1:c.519C>T (PRKRA)	NP_001303291.1:p.Gly173=
NM_003690.4:c.858C>T (PRKRA)	NP_003681.1:p.Gly286=
NR_110204.1:n.872-1201G>A (CHROMR)
NR_110205.1:n.716-1201G>A (CHROMR)
NR_110206.1:n.651-1201G>A (CHROMR)
XM_005246921.3:c.519C>T (PRKRA)	XP_005246978.1:p.Gly173=
XM_011512063.1:c.603C>T (PRKRA)	XP_011510365.1:p.Gly201=
XM_011512064.1:c.603C>T (PRKRA)	XP_011510366.1:p.Gly201=
XM_011512066.1:c.519C>T (PRKRA)	XP_011510368.1:p.Gly173=
XM_011512063.2:c.603C>T (PRKRA)	XP_011510365.1:p.Gly201=
XM_011512066.2:c.519C>T (PRKRA)	XP_011510368.1:p.Gly173=
XM_017005159.1:c.519C>T (PRKRA)	XP_016860648.1:p.Gly173=
XR_001739008.2:n.899C>T (PRKRA)
NM_003690.5:c.858C>T (PRKRA) MANE Select	NP_003681.1:p.Gly286=
NM_001316362.2:c.519C>T (PRKRA)	NP_001303291.1:p.Gly173=