Canonical Allele Identifier: CA013949
Gene: PRKAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181481
dbSNP Id: rs730880982

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151560556T>G , CM000669.2:g.151560556T>G GRCh38
NC_000007.13:g.151257642T>G , CM000669.1:g.151257642T>G GRCh37
NC_000007.12:g.150888575T>G NCBI36
NG_007486.1:g.321675A>C
NG_007486.2:g.321676A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000478989.7:c.*382A>C ENSP00000420645.3:n.*382A>C
ENST00000652321.2:c.1643A>C ENSP00000498886.2:p.Asp548Ala
ENST00000287878.9:c.1646A>C MANE Select ENSP00000287878.3:p.Asp549Ala
ENST00000476632.2:c.923A>C ENSP00000419493.2:p.Asp308Ala
ENST00000492843.6:c.1271A>C ENSP00000419577.2:p.Asp424Ala
ENST00000650664.1:n.1361A>C
ENST00000650851.1:n.1140A>C
ENST00000650858.1:c.863A>C ENSP00000498384.1:p.Asp288Ala
ENST00000650948.1:n.4032A>C
ENST00000651188.1:c.*759A>C ENSP00000498557.1:n.*759A>C
ENST00000651303.1:c.*965A>C ENSP00000498428.1:n.*965A>C
ENST00000651378.1:c.923A>C ENSP00000499103.1:p.Asp308Ala
ENST00000651764.1:c.1514A>C ENSP00000498796.1:p.Asp505Ala
ENST00000651836.1:c.1836A>C ENSP00000499156.1:n.1836A>C
ENST00000651954.1:n.1862A>C
ENST00000652047.1:c.1511A>C ENSP00000499111.1:p.Asp504Ala
ENST00000652136.1:n.2193A>C
ENST00000652159.1:c.1514A>C ENSP00000499025.1:p.Asp505Ala
ENST00000652397.1:c.*382A>C ENSP00000498351.1:n.*382A>C
ENST00000287878.8:c.1646A>C ENSP00000287878.3:p.Asp549Ala
ENST00000392801.6:c.1514A>C ENSP00000376549.2:p.Asp505Ala
ENST00000418337.6:c.923A>C ENSP00000387386.2:p.Asp308Ala
ENST00000479461.1:n.298A>C
ENST00000485183.1:n.299A>C
ENST00000492843.5:c.1274A>C ENSP00000419577.1:p.Asp425Ala
NM_001040633.1:c.1514A>C NP_001035723.1:p.Asp505Ala
NM_001304527.1:c.1271A>C NP_001291456.1:p.Asp424Ala
NM_001304531.1:c.923A>C NP_001291460.1:p.Asp308Ala
NM_016203.3:c.1646A>C NP_057287.2:p.Asp549Ala
NM_024429.1:c.923A>C NP_077747.1:p.Asp308Ala
XM_005250002.2:c.1646A>C XP_005250059.1:p.Asp549Ala
XM_005250004.2:c.1514A>C XP_005250061.1:p.Asp505Ala
XM_005250006.3:c.1274A>C XP_005250063.1:p.Asp425Ala
XM_006716021.2:c.1634A>C XP_006716084.1:p.Asp545Ala
XM_011516282.1:c.1631A>C XP_011514584.1:p.Asp544Ala
XM_011516283.1:c.1634A>C XP_011514585.1:p.Asp545Ala
XM_011516284.1:c.1631A>C XP_011514586.1:p.Asp544Ala
XM_011516285.1:c.923A>C XP_011514587.1:p.Asp308Ala
XM_011516286.1:c.899A>C XP_011514588.1:p.Asp300Ala
XM_011516287.1:c.863A>C XP_011514589.1:p.Asp288Ala
NM_001363698.1:c.1274A>C NP_001350627.1:p.Asp425Ala
XM_005250002.4:c.1646A>C XP_005250059.1:p.Asp549Ala
XM_005250004.4:c.1514A>C XP_005250061.1:p.Asp505Ala
XM_005250006.5:c.1274A>C XP_005250063.1:p.Asp425Ala
XM_011516285.2:c.923A>C XP_011514587.1:p.Asp308Ala
XM_011516286.2:c.899A>C XP_011514588.1:p.Asp300Ala
XM_017012268.2:c.1511A>C XP_016867757.1:p.Asp504Ala
XM_017012269.1:c.1643A>C XP_016867758.1:p.Asp548Ala
XM_017012270.1:c.1514A>C XP_016867759.1:p.Asp505Ala
XM_017012271.2:c.1511A>C XP_016867760.1:p.Asp504Ala
XM_017012272.1:c.1511A>C XP_016867761.1:p.Asp504Ala
XM_017012274.2:c.920A>C XP_016867763.1:p.Asp307Ala
XM_017012275.2:c.863A>C XP_016867764.1:p.Asp288Ala
XM_017012276.2:c.920A>C XP_016867765.1:p.Asp307Ala
XM_017012277.2:c.899A>C XP_016867766.1:p.Asp300Ala
XM_017012278.1:c.863A>C XP_016867767.1:p.Asp288Ala
XM_017012279.2:c.863A>C XP_016867768.1:p.Asp288Ala
XM_017012280.2:c.863A>C XP_016867769.1:p.Asp288Ala
XM_017012281.2:c.863A>C XP_016867770.1:p.Asp288Ala
XM_024446786.1:c.1514A>C XP_024302554.1:p.Asp505Ala
XM_024446787.1:c.923A>C XP_024302555.1:p.Asp308Ala
XM_024446788.1:c.920A>C XP_024302556.1:p.Asp307Ala
XM_024446789.1:c.923A>C XP_024302557.1:p.Asp308Ala
NM_016203.4:c.1646A>C MANE Select NP_057287.2:p.Asp549Ala
NM_001040633.2:c.1514A>C NP_001035723.1:p.Asp505Ala
NM_001304527.2:c.1271A>C NP_001291456.1:p.Asp424Ala
NM_001304531.2:c.923A>C NP_001291460.1:p.Asp308Ala
NM_001363698.2:c.1274A>C NP_001350627.1:p.Asp425Ala
NM_024429.2:c.923A>C NP_077747.1:p.Asp308Ala