Canonical Allele Identifier: CA370072176
Gene: PRKAG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151572698A>C , CM000669.2:g.151572698A>C GRCh38
NC_000007.13:g.151269784A>C , CM000669.1:g.151269784A>C GRCh37
NC_000007.12:g.150900717A>C NCBI36
NG_007486.1:g.309533T>G
NG_007486.2:g.309534T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000478989.7:c.291T>G ENSP00000420645.3:p.Tyr97Ter
ENST00000652321.2:c.1014T>G ENSP00000498886.2:p.Tyr338Ter
ENST00000287878.9:c.1017T>G MANE Select ENSP00000287878.3:p.Tyr339Ter
ENST00000476632.2:c.294T>G ENSP00000419493.2:p.Tyr98Ter
ENST00000478989.6:c.77T>G
ENST00000491938.6:n.360T>G
ENST00000492843.6:c.642T>G ENSP00000419577.2:p.Tyr214Ter
ENST00000650851.1:n.511T>G
ENST00000650858.1:c.234T>G ENSP00000498384.1:p.Tyr78Ter
ENST00000650948.1:n.1132T>G
ENST00000651188.1:c.*257T>G ENSP00000498557.1:n.*257T>G
ENST00000651290.1:n.160T>G
ENST00000651303.1:c.*336T>G ENSP00000498428.1:n.*336T>G
ENST00000651378.1:c.294T>G ENSP00000499103.1:p.Tyr98Ter
ENST00000651764.1:c.885T>G ENSP00000498796.1:p.Tyr295Ter
ENST00000651836.1:c.785T>G ENSP00000499156.1:n.785T>G
ENST00000652047.1:c.882T>G ENSP00000499111.1:p.Tyr294Ter
ENST00000652136.1:n.750T>G
ENST00000652159.1:c.885T>G ENSP00000499025.1:p.Tyr295Ter
ENST00000652397.1:c.294T>G ENSP00000498351.1:p.Tyr98Ter
ENST00000287878.8:c.1017T>G ENSP00000287878.3:p.Tyr339Ter
ENST00000392801.6:c.885T>G ENSP00000376549.2:p.Tyr295Ter
ENST00000418337.6:c.294T>G ENSP00000387386.2:p.Tyr98Ter
ENST00000476632.1:c.294T>G ENSP00000419493.1:p.Tyr98Ter
ENST00000478989.5:c.69T>G ENSP00000420645.1:p.Tyr23Ter
ENST00000488258.5:c.*257T>G ENSP00000420783.1:n.*257T>G
ENST00000491938.5:n.363T>G
ENST00000492843.5:c.645T>G ENSP00000419577.1:p.Tyr215Ter
ENST00000493872.5:c.*266T>G ENSP00000417252.1:n.*266T>G
NM_001040633.1:c.885T>G NP_001035723.1:p.Tyr295Ter
NM_001304527.1:c.642T>G NP_001291456.1:p.Tyr214Ter
NM_001304531.1:c.294T>G NP_001291460.1:p.Tyr98Ter
NM_016203.3:c.1017T>G NP_057287.2:p.Tyr339Ter
NM_024429.1:c.294T>G NP_077747.1:p.Tyr98Ter
XM_005250002.2:c.1017T>G XP_005250059.1:p.Tyr339Ter
XM_005250004.2:c.885T>G XP_005250061.1:p.Tyr295Ter
XM_005250006.3:c.645T>G XP_005250063.1:p.Tyr215Ter
XM_006716021.2:c.1005T>G XP_006716084.1:p.Tyr335Ter
XM_011516282.1:c.1002T>G XP_011514584.1:p.Tyr334Ter
XM_011516283.1:c.1005T>G XP_011514585.1:p.Tyr335Ter
XM_011516284.1:c.1002T>G XP_011514586.1:p.Tyr334Ter
XM_011516285.1:c.294T>G XP_011514587.1:p.Tyr98Ter
XM_011516286.1:c.270T>G XP_011514588.1:p.Tyr90Ter
XM_011516287.1:c.234T>G XP_011514589.1:p.Tyr78Ter
NM_001363698.1:c.645T>G NP_001350627.1:p.Tyr215Ter
XM_005250002.4:c.1017T>G XP_005250059.1:p.Tyr339Ter
XM_005250004.4:c.885T>G XP_005250061.1:p.Tyr295Ter
XM_005250006.5:c.645T>G XP_005250063.1:p.Tyr215Ter
XM_011516285.2:c.294T>G XP_011514587.1:p.Tyr98Ter
XM_011516286.2:c.270T>G XP_011514588.1:p.Tyr90Ter
XM_017012268.2:c.882T>G XP_016867757.1:p.Tyr294Ter
XM_017012269.1:c.1014T>G XP_016867758.1:p.Tyr338Ter
XM_017012270.1:c.885T>G XP_016867759.1:p.Tyr295Ter
XM_017012271.2:c.882T>G XP_016867760.1:p.Tyr294Ter
XM_017012272.1:c.882T>G XP_016867761.1:p.Tyr294Ter
XM_017012274.2:c.291T>G XP_016867763.1:p.Tyr97Ter
XM_017012275.2:c.234T>G XP_016867764.1:p.Tyr78Ter
XM_017012276.2:c.291T>G XP_016867765.1:p.Tyr97Ter
XM_017012277.2:c.270T>G XP_016867766.1:p.Tyr90Ter
XM_017012278.1:c.234T>G XP_016867767.1:p.Tyr78Ter
XM_017012279.2:c.234T>G XP_016867768.1:p.Tyr78Ter
XM_017012280.2:c.234T>G XP_016867769.1:p.Tyr78Ter
XM_017012281.2:c.234T>G XP_016867770.1:p.Tyr78Ter
XM_024446786.1:c.885T>G XP_024302554.1:p.Tyr295Ter
XM_024446787.1:c.294T>G XP_024302555.1:p.Tyr98Ter
XM_024446788.1:c.291T>G XP_024302556.1:p.Tyr97Ter
XM_024446789.1:c.294T>G XP_024302557.1:p.Tyr98Ter
NM_016203.4:c.1017T>G MANE Select NP_057287.2:p.Tyr339Ter
NM_001040633.2:c.885T>G NP_001035723.1:p.Tyr295Ter
NM_001304527.2:c.642T>G NP_001291456.1:p.Tyr214Ter
NM_001304531.2:c.294T>G NP_001291460.1:p.Tyr98Ter
NM_001363698.2:c.645T>G NP_001350627.1:p.Tyr215Ter
NM_024429.2:c.294T>G NP_077747.1:p.Tyr98Ter