Canonical Allele Identifier: CA370072195
Gene: PRKAG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151572705T>G , CM000669.2:g.151572705T>G GRCh38
NC_000007.13:g.151269791T>G , CM000669.1:g.151269791T>G GRCh37
NC_000007.12:g.150900724T>G NCBI36
NG_007486.1:g.309526A>C
NG_007486.2:g.309527A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478989.7:c.284A>C ENSP00000420645.3:p.Gln95Pro
ENST00000652321.2:c.1007A>C ENSP00000498886.2:p.Gln336Pro
ENST00000287878.9:c.1010A>C MANE Select ENSP00000287878.3:p.Gln337Pro
ENST00000476632.2:c.287A>C ENSP00000419493.2:p.Gln96Pro
ENST00000478989.6:c.70A>C
ENST00000491938.6:n.353A>C
ENST00000492843.6:c.635A>C ENSP00000419577.2:p.Gln212Pro
ENST00000650851.1:n.504A>C
ENST00000650858.1:c.227A>C ENSP00000498384.1:p.Gln76Pro
ENST00000650948.1:n.1125A>C
ENST00000651188.1:c.*250A>C ENSP00000498557.1:n.*250A>C
ENST00000651290.1:n.153A>C
ENST00000651303.1:c.*329A>C ENSP00000498428.1:n.*329A>C
ENST00000651378.1:c.287A>C ENSP00000499103.1:p.Gln96Pro
ENST00000651764.1:c.878A>C ENSP00000498796.1:p.Gln293Pro
ENST00000651836.1:c.778A>C ENSP00000499156.1:n.778A>C
ENST00000652047.1:c.875A>C ENSP00000499111.1:p.Gln292Pro
ENST00000652136.1:n.743A>C
ENST00000652159.1:c.878A>C ENSP00000499025.1:p.Gln293Pro
ENST00000652397.1:c.287A>C ENSP00000498351.1:p.Gln96Pro
ENST00000287878.8:c.1010A>C ENSP00000287878.3:p.Gln337Pro
ENST00000392801.6:c.878A>C ENSP00000376549.2:p.Gln293Pro
ENST00000418337.6:c.287A>C ENSP00000387386.2:p.Gln96Pro
ENST00000476632.1:c.287A>C ENSP00000419493.1:p.Gln96Pro
ENST00000478989.5:c.62A>C ENSP00000420645.1:p.Gln21Pro
ENST00000488258.5:c.*250A>C ENSP00000420783.1:n.*250A>C
ENST00000491938.5:n.356A>C
ENST00000492843.5:c.638A>C ENSP00000419577.1:p.Gln213Pro
ENST00000493872.5:c.*259A>C ENSP00000417252.1:n.*259A>C
NM_001040633.1:c.878A>C NP_001035723.1:p.Gln293Pro
NM_001304527.1:c.635A>C NP_001291456.1:p.Gln212Pro
NM_001304531.1:c.287A>C NP_001291460.1:p.Gln96Pro
NM_016203.3:c.1010A>C NP_057287.2:p.Gln337Pro
NM_024429.1:c.287A>C NP_077747.1:p.Gln96Pro
XM_005250002.2:c.1010A>C XP_005250059.1:p.Gln337Pro
XM_005250004.2:c.878A>C XP_005250061.1:p.Gln293Pro
XM_005250006.3:c.638A>C XP_005250063.1:p.Gln213Pro
XM_006716021.2:c.998A>C XP_006716084.1:p.Gln333Pro
XM_011516282.1:c.995A>C XP_011514584.1:p.Gln332Pro
XM_011516283.1:c.998A>C XP_011514585.1:p.Gln333Pro
XM_011516284.1:c.995A>C XP_011514586.1:p.Gln332Pro
XM_011516285.1:c.287A>C XP_011514587.1:p.Gln96Pro
XM_011516286.1:c.263A>C XP_011514588.1:p.Gln88Pro
XM_011516287.1:c.227A>C XP_011514589.1:p.Gln76Pro
NM_001363698.1:c.638A>C NP_001350627.1:p.Gln213Pro
XM_005250002.4:c.1010A>C XP_005250059.1:p.Gln337Pro
XM_005250004.4:c.878A>C XP_005250061.1:p.Gln293Pro
XM_005250006.5:c.638A>C XP_005250063.1:p.Gln213Pro
XM_011516285.2:c.287A>C XP_011514587.1:p.Gln96Pro
XM_011516286.2:c.263A>C XP_011514588.1:p.Gln88Pro
XM_017012268.2:c.875A>C XP_016867757.1:p.Gln292Pro
XM_017012269.1:c.1007A>C XP_016867758.1:p.Gln336Pro
XM_017012270.1:c.878A>C XP_016867759.1:p.Gln293Pro
XM_017012271.2:c.875A>C XP_016867760.1:p.Gln292Pro
XM_017012272.1:c.875A>C XP_016867761.1:p.Gln292Pro
XM_017012274.2:c.284A>C XP_016867763.1:p.Gln95Pro
XM_017012275.2:c.227A>C XP_016867764.1:p.Gln76Pro
XM_017012276.2:c.284A>C XP_016867765.1:p.Gln95Pro
XM_017012277.2:c.263A>C XP_016867766.1:p.Gln88Pro
XM_017012278.1:c.227A>C XP_016867767.1:p.Gln76Pro
XM_017012279.2:c.227A>C XP_016867768.1:p.Gln76Pro
XM_017012280.2:c.227A>C XP_016867769.1:p.Gln76Pro
XM_017012281.2:c.227A>C XP_016867770.1:p.Gln76Pro
XM_024446786.1:c.878A>C XP_024302554.1:p.Gln293Pro
XM_024446787.1:c.287A>C XP_024302555.1:p.Gln96Pro
XM_024446788.1:c.284A>C XP_024302556.1:p.Gln95Pro
XM_024446789.1:c.287A>C XP_024302557.1:p.Gln96Pro
NM_016203.4:c.1010A>C MANE Select NP_057287.2:p.Gln337Pro
NM_001040633.2:c.878A>C NP_001035723.1:p.Gln293Pro
NM_001304527.2:c.635A>C NP_001291456.1:p.Gln212Pro
NM_001304531.2:c.287A>C NP_001291460.1:p.Gln96Pro
NM_001363698.2:c.638A>C NP_001350627.1:p.Gln213Pro
NM_024429.2:c.287A>C NP_077747.1:p.Gln96Pro