Canonical Allele Identifier: CA1752708231
Gene: PRKAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151556999_151557001delinsAAC , CM000669.2:g.151556999_151557001delinsAAC GRCh38
NC_000007.13:g.151254085_151254087delinsAAC , CM000669.1:g.151254085_151254087delinsAAC GRCh37
NC_000007.12:g.150885018_150885020delinsAAC NCBI36
NG_007486.1:g.325230_325232delinsGTT
NG_007486.2:g.325231_325233delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000478989.7:c.*646_*648delinsGTT ENSP00000420645.3:n.*646_*648delinsGTT
ENST00000652321.2:c.*200_*202delinsGTT ENSP00000498886.2:n.*200_*202delinsGTT
ENST00000287878.9:c.*200_*202delinsGTT MANE Select ENSP00000287878.3:n.*200_*202delinsGTT
ENST00000476632.2:c.*200_*202delinsGTT ENSP00000419493.2:n.*200_*202delinsGTT
ENST00000492843.6:c.*200_*202delinsGTT ENSP00000419577.2:n.*200_*202delinsGTT
ENST00000650664.1:n.1625_1627delinsGTT
ENST00000650851.1:n.1404_1406delinsGTT
ENST00000650858.1:c.*200_*202delinsGTT ENSP00000498384.1:n.*200_*202delinsGTT
ENST00000650948.1:n.4296_4298delinsGTT
ENST00000651188.1:c.*1023_*1025delinsGTT ENSP00000498557.1:n.*1023_*1025delinsGTT
ENST00000651303.1:c.*1229_*1231delinsGTT ENSP00000498428.1:n.*1229_*1231delinsGTT
ENST00000651378.1:c.*200_*202delinsGTT ENSP00000499103.1:n.*200_*202delinsGTT
ENST00000651764.1:c.*200_*202delinsGTT ENSP00000498796.1:n.*200_*202delinsGTT
ENST00000651836.1:c.2100_2102delinsGTT ENSP00000499156.1:n.2100_2102delinsGTT
ENST00000651954.1:n.2126_2128delinsGTT
ENST00000652136.1:n.2457_2459delinsGTT
ENST00000652159.1:c.*200_*202delinsGTT ENSP00000499025.1:n.*200_*202delinsGTT
ENST00000652397.1:c.*646_*648delinsGTT ENSP00000498351.1:n.*646_*648delinsGTT
ENST00000287878.8:c.*200_*202delinsGTT ENSP00000287878.3:n.*200_*202delinsGTT
ENST00000392801.6:c.*200_*202delinsGTT ENSP00000376549.2:n.*200_*202delinsGTT
ENST00000418337.6:c.*200_*202delinsGTT ENSP00000387386.2:n.*200_*202delinsGTT
ENST00000479461.1:n.562_564delinsGTT
ENST00000492843.5:c.*200_*202delinsGTT ENSP00000419577.1:n.*200_*202delinsGTT
NM_001040633.1:c.*200_*202delinsGTT NP_001035723.1:n.*200_*202delinsGTT
NM_001304527.1:c.*200_*202delinsGTT NP_001291456.1:n.*200_*202delinsGTT
NM_001304531.1:c.*200_*202delinsGTT NP_001291460.1:n.*200_*202delinsGTT
NM_016203.3:c.*200_*202delinsGTT NP_057287.2:n.*200_*202delinsGTT
NM_024429.1:c.*200_*202delinsGTT NP_077747.1:n.*200_*202delinsGTT
XM_005250002.2:c.*3341_*3343delinsGTT XP_005250059.1:n.*3341_*3343delinsGTT
XM_005250004.2:c.*3341_*3343delinsGTT XP_005250061.1:n.*3341_*3343delinsGTT
XM_005250006.3:c.*3341_*3343delinsGTT XP_005250063.1:n.*3341_*3343delinsGTT
XM_006716021.2:c.*3341_*3343delinsGTT XP_006716084.1:n.*3341_*3343delinsGTT
XM_011516282.1:c.*3341_*3343delinsGTT XP_011514584.1:n.*3341_*3343delinsGTT
XM_011516283.1:c.*200_*202delinsGTT XP_011514585.1:n.*200_*202delinsGTT
XM_011516284.1:c.*200_*202delinsGTT XP_011514586.1:n.*200_*202delinsGTT
XM_011516285.1:c.*3341_*3343delinsGTT XP_011514587.1:n.*3341_*3343delinsGTT
XM_011516286.1:c.*3341_*3343delinsGTT XP_011514588.1:n.*3341_*3343delinsGTT
XM_011516287.1:c.*3341_*3343delinsGTT XP_011514589.1:n.*3341_*3343delinsGTT
NM_001363698.1:c.*200_*202delinsGTT NP_001350627.1:n.*200_*202delinsGTT
XM_005250002.4:c.*3341_*3343delinsGTT XP_005250059.1:n.*3341_*3343delinsGTT
XM_005250004.4:c.*3341_*3343delinsGTT XP_005250061.1:n.*3341_*3343delinsGTT
XM_005250006.5:c.*3341_*3343delinsGTT XP_005250063.1:n.*3341_*3343delinsGTT
XM_011516285.2:c.*3341_*3343delinsGTT XP_011514587.1:n.*3341_*3343delinsGTT
XM_011516286.2:c.*3341_*3343delinsGTT XP_011514588.1:n.*3341_*3343delinsGTT
XM_017012268.2:c.*3341_*3343delinsGTT XP_016867757.1:n.*3341_*3343delinsGTT
XM_017012269.1:c.*200_*202delinsGTT XP_016867758.1:n.*200_*202delinsGTT
XM_017012270.1:c.*200_*202delinsGTT XP_016867759.1:n.*200_*202delinsGTT
XM_017012271.2:c.*200_*202delinsGTT XP_016867760.1:n.*200_*202delinsGTT
XM_017012272.1:c.*200_*202delinsGTT XP_016867761.1:n.*200_*202delinsGTT
XM_017012274.2:c.*3341_*3343delinsGTT XP_016867763.1:n.*3341_*3343delinsGTT
XM_017012275.2:c.*3341_*3343delinsGTT XP_016867764.1:n.*3341_*3343delinsGTT
XM_017012276.2:c.*200_*202delinsGTT XP_016867765.1:n.*200_*202delinsGTT
XM_017012277.2:c.*200_*202delinsGTT XP_016867766.1:n.*200_*202delinsGTT
XM_017012278.1:c.*200_*202delinsGTT XP_016867767.1:n.*200_*202delinsGTT
XM_017012279.2:c.*200_*202delinsGTT XP_016867768.1:n.*200_*202delinsGTT
XM_017012280.2:c.*200_*202delinsGTT XP_016867769.1:n.*200_*202delinsGTT
XM_017012281.2:c.*200_*202delinsGTT XP_016867770.1:n.*200_*202delinsGTT
XM_024446786.1:c.*3341_*3343delinsGTT XP_024302554.1:n.*3341_*3343delinsGTT
XM_024446787.1:c.*3341_*3343delinsGTT XP_024302555.1:n.*3341_*3343delinsGTT
XM_024446788.1:c.*3341_*3343delinsGTT XP_024302556.1:n.*3341_*3343delinsGTT
XM_024446789.1:c.*200_*202delinsGTT XP_024302557.1:n.*200_*202delinsGTT
NM_016203.4:c.*200_*202delinsGTT MANE Select NP_057287.2:n.*200_*202delinsGTT
NM_001040633.2:c.*200_*202delinsGTT NP_001035723.1:n.*200_*202delinsGTT
NM_001304527.2:c.*200_*202delinsGTT NP_001291456.1:n.*200_*202delinsGTT
NM_001304531.2:c.*200_*202delinsGTT NP_001291460.1:n.*200_*202delinsGTT
NM_001363698.2:c.*200_*202delinsGTT NP_001350627.1:n.*200_*202delinsGTT
NM_024429.2:c.*200_*202delinsGTT NP_077747.1:n.*200_*202delinsGTT