Canonical Allele Identifier: CA370072120
Gene: PRKAG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151572676C>A , CM000669.2:g.151572676C>A GRCh38
NC_000007.13:g.151269762C>A , CM000669.1:g.151269762C>A GRCh37
NC_000007.12:g.150900695C>A NCBI36
NG_007486.1:g.309555G>T
NG_007486.2:g.309556G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478989.7:c.313G>T ENSP00000420645.3:p.Glu105Ter
ENST00000652321.2:c.1036G>T ENSP00000498886.2:p.Glu346Ter
ENST00000287878.9:c.1039G>T MANE Select ENSP00000287878.3:p.Glu347Ter
ENST00000476632.2:c.316G>T ENSP00000419493.2:p.Glu106Ter
ENST00000478989.6:c.99G>T
ENST00000491938.6:n.382G>T
ENST00000492843.6:c.664G>T ENSP00000419577.2:p.Glu222Ter
ENST00000650851.1:n.533G>T
ENST00000650858.1:c.256G>T ENSP00000498384.1:p.Glu86Ter
ENST00000650948.1:n.1154G>T
ENST00000651188.1:c.*279G>T ENSP00000498557.1:n.*279G>T
ENST00000651290.1:n.182G>T
ENST00000651303.1:c.*358G>T ENSP00000498428.1:n.*358G>T
ENST00000651378.1:c.316G>T ENSP00000499103.1:p.Glu106Ter
ENST00000651764.1:c.907G>T ENSP00000498796.1:p.Glu303Ter
ENST00000651836.1:c.807G>T ENSP00000499156.1:n.807G>T
ENST00000652047.1:c.904G>T ENSP00000499111.1:p.Glu302Ter
ENST00000652136.1:n.772G>T
ENST00000652159.1:c.907G>T ENSP00000499025.1:p.Glu303Ter
ENST00000652397.1:c.316G>T ENSP00000498351.1:p.Glu106Ter
ENST00000287878.8:c.1039G>T ENSP00000287878.3:p.Glu347Ter
ENST00000392801.6:c.907G>T ENSP00000376549.2:p.Glu303Ter
ENST00000418337.6:c.316G>T ENSP00000387386.2:p.Glu106Ter
ENST00000476632.1:c.316G>T ENSP00000419493.1:p.Glu106Ter
ENST00000478989.5:c.91G>T ENSP00000420645.1:p.Glu31Ter
ENST00000488258.5:c.*279G>T ENSP00000420783.1:n.*279G>T
ENST00000491938.5:n.385G>T
ENST00000492843.5:c.667G>T ENSP00000419577.1:p.Glu223Ter
ENST00000493872.5:c.*288G>T ENSP00000417252.1:n.*288G>T
NM_001040633.1:c.907G>T NP_001035723.1:p.Glu303Ter
NM_001304527.1:c.664G>T NP_001291456.1:p.Glu222Ter
NM_001304531.1:c.316G>T NP_001291460.1:p.Glu106Ter
NM_016203.3:c.1039G>T NP_057287.2:p.Glu347Ter
NM_024429.1:c.316G>T NP_077747.1:p.Glu106Ter
XM_005250002.2:c.1039G>T XP_005250059.1:p.Glu347Ter
XM_005250004.2:c.907G>T XP_005250061.1:p.Glu303Ter
XM_005250006.3:c.667G>T XP_005250063.1:p.Glu223Ter
XM_006716021.2:c.1027G>T XP_006716084.1:p.Glu343Ter
XM_011516282.1:c.1024G>T XP_011514584.1:p.Glu342Ter
XM_011516283.1:c.1027G>T XP_011514585.1:p.Glu343Ter
XM_011516284.1:c.1024G>T XP_011514586.1:p.Glu342Ter
XM_011516285.1:c.316G>T XP_011514587.1:p.Glu106Ter
XM_011516286.1:c.292G>T XP_011514588.1:p.Glu98Ter
XM_011516287.1:c.256G>T XP_011514589.1:p.Glu86Ter
NM_001363698.1:c.667G>T NP_001350627.1:p.Glu223Ter
XM_005250002.4:c.1039G>T XP_005250059.1:p.Glu347Ter
XM_005250004.4:c.907G>T XP_005250061.1:p.Glu303Ter
XM_005250006.5:c.667G>T XP_005250063.1:p.Glu223Ter
XM_011516285.2:c.316G>T XP_011514587.1:p.Glu106Ter
XM_011516286.2:c.292G>T XP_011514588.1:p.Glu98Ter
XM_017012268.2:c.904G>T XP_016867757.1:p.Glu302Ter
XM_017012269.1:c.1036G>T XP_016867758.1:p.Glu346Ter
XM_017012270.1:c.907G>T XP_016867759.1:p.Glu303Ter
XM_017012271.2:c.904G>T XP_016867760.1:p.Glu302Ter
XM_017012272.1:c.904G>T XP_016867761.1:p.Glu302Ter
XM_017012274.2:c.313G>T XP_016867763.1:p.Glu105Ter
XM_017012275.2:c.256G>T XP_016867764.1:p.Glu86Ter
XM_017012276.2:c.313G>T XP_016867765.1:p.Glu105Ter
XM_017012277.2:c.292G>T XP_016867766.1:p.Glu98Ter
XM_017012278.1:c.256G>T XP_016867767.1:p.Glu86Ter
XM_017012279.2:c.256G>T XP_016867768.1:p.Glu86Ter
XM_017012280.2:c.256G>T XP_016867769.1:p.Glu86Ter
XM_017012281.2:c.256G>T XP_016867770.1:p.Glu86Ter
XM_024446786.1:c.907G>T XP_024302554.1:p.Glu303Ter
XM_024446787.1:c.316G>T XP_024302555.1:p.Glu106Ter
XM_024446788.1:c.313G>T XP_024302556.1:p.Glu105Ter
XM_024446789.1:c.316G>T XP_024302557.1:p.Glu106Ter
NM_016203.4:c.1039G>T MANE Select NP_057287.2:p.Glu347Ter
NM_001040633.2:c.907G>T NP_001035723.1:p.Glu303Ter
NM_001304527.2:c.664G>T NP_001291456.1:p.Glu222Ter
NM_001304531.2:c.316G>T NP_001291460.1:p.Glu106Ter
NM_001363698.2:c.667G>T NP_001350627.1:p.Glu223Ter
NM_024429.2:c.316G>T NP_077747.1:p.Glu106Ter