Canonical Allele Identifier: CA430089868

Gene: PRKRA CHROMR

Linked Data

• gnomAD v4: 2-178432205-G-T
• MyVariant Identifiers: chr2:g.179296932G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432205G>T , CM000664.2:g.178432205G>T	GRCh38
NC_000002.11:g.179296932G>T , CM000664.1:g.179296932G>T	GRCh37
NC_000002.10:g.179005178G>T	NCBI36
NG_009053.1:g.24027C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.834C>A (PRKRA) MANE Select	ENSP00000318176.4:p.Thr278=
ENST00000448279.2:c.*562C>A (PRKRA)	ENSP00000388455.1:n.*562C>A
ENST00000457633.2:c.*338C>A (PRKRA)	ENSP00000408668.2:n.*338C>A
ENST00000474793.6:n.975C>A (PRKRA)
ENST00000676505.1:c.*594C>A (PRKRA)	ENSP00000504163.1:n.*594C>A
ENST00000676586.1:n.2971C>A (PRKRA)
ENST00000676752.1:n.2733C>A (PRKRA)
ENST00000676832.1:c.*655C>A (PRKRA)	ENSP00000503231.1:n.*655C>A
ENST00000676922.1:c.*562C>A (PRKRA)	ENSP00000503369.1:n.*562C>A
ENST00000677136.1:n.2826C>A (PRKRA)
ENST00000677206.1:c.*626C>A (PRKRA)	ENSP00000503034.1:n.*626C>A
ENST00000677253.1:c.*531C>A (PRKRA)	ENSP00000503466.1:n.*531C>A
ENST00000677386.1:c.*277C>A (PRKRA)	ENSP00000503003.1:n.*277C>A
ENST00000677460.1:c.*163C>A (PRKRA)	ENSP00000504507.1:n.*163C>A
ENST00000677584.1:c.*672C>A (PRKRA)	ENSP00000504411.1:n.*672C>A
ENST00000677689.1:c.579C>A (PRKRA)	ENSP00000502919.1:p.Thr193=
ENST00000677859.1:c.687C>A (PRKRA)
ENST00000677981.1:c.582C>A (PRKRA)	ENSP00000503536.1:p.Thr194=
ENST00000678053.1:c.*594C>A (PRKRA)	ENSP00000504330.1:n.*594C>A
ENST00000678058.1:c.578C>A (PRKRA)	ENSP00000503203.1:n.578C>A
ENST00000678167.1:c.*388C>A (PRKRA)	ENSP00000504479.1:n.*388C>A
ENST00000678775.1:c.495C>A (PRKRA)	ENSP00000504030.1:p.Thr165=
ENST00000678845.1:c.495C>A (PRKRA)	ENSP00000503011.1:p.Thr165=
ENST00000679037.1:c.*502C>A (PRKRA)	ENSP00000504421.1:n.*502C>A
ENST00000679202.1:n.1921C>A (PRKRA)
ENST00000325748.8:c.834C>A (PRKRA)	ENSP00000318176.4:p.Thr278=
ENST00000424699.5:c.*626C>A (PRKRA)	ENSP00000408029.1:n.*626C>A
ENST00000432031.6:c.801C>A (PRKRA)	ENSP00000393883.2:p.Thr267=
ENST00000487082.5:c.759C>A (PRKRA)	ENSP00000430604.1:p.Thr253=
ENST00000490501.5:n.1061C>A (PRKRA)
NM_001139517.1:c.801C>A (PRKRA)	NP_001132989.1:p.Thr267=
NM_001139518.1:c.759C>A (PRKRA)	NP_001132990.1:p.Thr253=
NM_001316362.1:c.495C>A (PRKRA)	NP_001303291.1:p.Thr165=
NM_003690.4:c.834C>A (PRKRA)	NP_003681.1:p.Thr278=
NR_110204.1:n.872-1177G>T (CHROMR)
NR_110205.1:n.716-1177G>T (CHROMR)
NR_110206.1:n.651-1177G>T (CHROMR)
XM_005246921.3:c.495C>A (PRKRA)	XP_005246978.1:p.Thr165=
XM_011512063.1:c.579C>A (PRKRA)	XP_011510365.1:p.Thr193=
XM_011512064.1:c.579C>A (PRKRA)	XP_011510366.1:p.Thr193=
XM_011512066.1:c.495C>A (PRKRA)	XP_011510368.1:p.Thr165=
XM_011512063.2:c.579C>A (PRKRA)	XP_011510365.1:p.Thr193=
XM_011512066.2:c.495C>A (PRKRA)	XP_011510368.1:p.Thr165=
XM_017005159.1:c.495C>A (PRKRA)	XP_016860648.1:p.Thr165=
XR_001739008.2:n.875C>A (PRKRA)
NM_003690.5:c.834C>A (PRKRA) MANE Select	NP_003681.1:p.Thr278=
NM_001316362.2:c.495C>A (PRKRA)	NP_001303291.1:p.Thr165=