Canonical Allele Identifier: CA458663414

Gene: PRKAG2

Linked Data

• MyVariant Identifiers: chr7:g.151261179T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151564093T>C , CM000669.2:g.151564093T>C	GRCh38
NC_000007.13:g.151261179T>C , CM000669.1:g.151261179T>C	GRCh37
NC_000007.12:g.150892112T>C	NCBI36
NG_007486.1:g.318138A>G
NG_007486.2:g.318139A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000478989.7:c.*305A>G	ENSP00000420645.3:n.*305A>G
ENST00000652321.2:c.1566A>G	ENSP00000498886.2:p.Arg522=
ENST00000287878.9:c.1569A>G MANE Select	ENSP00000287878.3:p.Arg523=
ENST00000476632.2:c.846A>G	ENSP00000419493.2:p.Arg282=
ENST00000492843.6:c.1194A>G	ENSP00000419577.2:p.Arg398=
ENST00000650851.1:n.1063A>G
ENST00000650858.1:c.786A>G	ENSP00000498384.1:p.Arg262=
ENST00000650948.1:n.3955A>G
ENST00000651188.1:c.*682A>G	ENSP00000498557.1:n.*682A>G
ENST00000651303.1:c.*888A>G	ENSP00000498428.1:n.*888A>G
ENST00000651378.1:c.846A>G	ENSP00000499103.1:p.Arg282=
ENST00000651764.1:c.1437A>G	ENSP00000498796.1:p.Arg479=
ENST00000651836.1:c.1759A>G	ENSP00000499156.1:n.1759A>G
ENST00000651954.1:n.1785A>G
ENST00000652047.1:c.1434A>G	ENSP00000499111.1:p.Arg478=
ENST00000652136.1:n.2116A>G
ENST00000652159.1:c.1437A>G	ENSP00000499025.1:p.Arg479=
ENST00000652397.1:c.*305A>G	ENSP00000498351.1:n.*305A>G
ENST00000287878.8:c.1569A>G	ENSP00000287878.3:p.Arg523=
ENST00000392801.6:c.1437A>G	ENSP00000376549.2:p.Arg479=
ENST00000418337.6:c.846A>G	ENSP00000387386.2:p.Arg282=
ENST00000479461.1:n.221A>G
ENST00000485183.1:n.222A>G
ENST00000492843.5:c.1197A>G	ENSP00000419577.1:p.Arg399=
NM_001040633.1:c.1437A>G	NP_001035723.1:p.Arg479=
NM_001304527.1:c.1194A>G	NP_001291456.1:p.Arg398=
NM_001304531.1:c.846A>G	NP_001291460.1:p.Arg282=
NM_016203.3:c.1569A>G	NP_057287.2:p.Arg523=
NM_024429.1:c.846A>G	NP_077747.1:p.Arg282=
XM_005250002.2:c.1569A>G	XP_005250059.1:p.Arg523=
XM_005250004.2:c.1437A>G	XP_005250061.1:p.Arg479=
XM_005250006.3:c.1197A>G	XP_005250063.1:p.Arg399=
XM_006716021.2:c.1557A>G	XP_006716084.1:p.Arg519=
XM_011516282.1:c.1554A>G	XP_011514584.1:p.Arg518=
XM_011516283.1:c.1557A>G	XP_011514585.1:p.Arg519=
XM_011516284.1:c.1554A>G	XP_011514586.1:p.Arg518=
XM_011516285.1:c.846A>G	XP_011514587.1:p.Arg282=
XM_011516286.1:c.822A>G	XP_011514588.1:p.Arg274=
XM_011516287.1:c.786A>G	XP_011514589.1:p.Arg262=
NM_001363698.1:c.1197A>G	NP_001350627.1:p.Arg399=
XM_005250002.4:c.1569A>G	XP_005250059.1:p.Arg523=
XM_005250004.4:c.1437A>G	XP_005250061.1:p.Arg479=
XM_005250006.5:c.1197A>G	XP_005250063.1:p.Arg399=
XM_011516285.2:c.846A>G	XP_011514587.1:p.Arg282=
XM_011516286.2:c.822A>G	XP_011514588.1:p.Arg274=
XM_017012268.2:c.1434A>G	XP_016867757.1:p.Arg478=
XM_017012269.1:c.1566A>G	XP_016867758.1:p.Arg522=
XM_017012270.1:c.1437A>G	XP_016867759.1:p.Arg479=
XM_017012271.2:c.1434A>G	XP_016867760.1:p.Arg478=
XM_017012272.1:c.1434A>G	XP_016867761.1:p.Arg478=
XM_017012274.2:c.843A>G	XP_016867763.1:p.Arg281=
XM_017012275.2:c.786A>G	XP_016867764.1:p.Arg262=
XM_017012276.2:c.843A>G	XP_016867765.1:p.Arg281=
XM_017012277.2:c.822A>G	XP_016867766.1:p.Arg274=
XM_017012278.1:c.786A>G	XP_016867767.1:p.Arg262=
XM_017012279.2:c.786A>G	XP_016867768.1:p.Arg262=
XM_017012280.2:c.786A>G	XP_016867769.1:p.Arg262=
XM_017012281.2:c.786A>G	XP_016867770.1:p.Arg262=
XM_024446786.1:c.1437A>G	XP_024302554.1:p.Arg479=
XM_024446787.1:c.846A>G	XP_024302555.1:p.Arg282=
XM_024446788.1:c.843A>G	XP_024302556.1:p.Arg281=
XM_024446789.1:c.846A>G	XP_024302557.1:p.Arg282=
NM_016203.4:c.1569A>G MANE Select	NP_057287.2:p.Arg523=
NM_001040633.2:c.1437A>G	NP_001035723.1:p.Arg479=
NM_001304527.2:c.1194A>G	NP_001291456.1:p.Arg398=
NM_001304531.2:c.846A>G	NP_001291460.1:p.Arg282=
NM_001363698.2:c.1197A>G	NP_001350627.1:p.Arg399=
NM_024429.2:c.846A>G	NP_077747.1:p.Arg282=