Canonical Allele Identifier: CA2697549710
Gene: PRKAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2745337
ClinVar RCV Id: RCV003506870

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151576441_151576447del , CM000669.2:g.151576441_151576447del GRCh38
NC_000007.13:g.151273527_151273533del , CM000669.1:g.151273527_151273533del GRCh37
NC_000007.12:g.150904460_150904466del NCBI36
NG_007486.1:g.305784_305790del
NG_007486.2:g.305785_305791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000478989.7:c.144_150del ENSP00000420645.3:p.Lys48AsnfsTer6
ENST00000652321.2:c.867_873del ENSP00000498886.2:p.Lys289AsnfsTer6
ENST00000287878.9:c.870_876del MANE Select ENSP00000287878.3:p.Lys290AsnfsTer6
ENST00000476632.2:c.147_153del ENSP00000419493.2:p.Lys49AsnfsTer6
ENST00000491938.6:n.213_219del
ENST00000492843.6:c.495_501del ENSP00000419577.2:p.Lys165AsnfsTer6
ENST00000650851.1:n.364_370del
ENST00000650858.1:c.87_93del ENSP00000498384.1:p.Lys29AsnfsTer6
ENST00000650948.1:n.985_991del
ENST00000651188.1:c.*110_*116del ENSP00000498557.1:n.*110_*116del
ENST00000651290.1:n.72_78del
ENST00000651303.1:c.*189_*195del ENSP00000498428.1:n.*189_*195del
ENST00000651378.1:c.147_153del ENSP00000499103.1:p.Lys49AsnfsTer6
ENST00000651764.1:c.738_744del ENSP00000498796.1:p.Lys246AsnfsTer6
ENST00000651836.1:c.638_644del ENSP00000499156.1:n.638_644del
ENST00000652047.1:c.735_741del ENSP00000499111.1:p.Lys245AsnfsTer6
ENST00000652136.1:n.603_609del
ENST00000652159.1:c.738_744del ENSP00000499025.1:p.Lys246AsnfsTer6
ENST00000652397.1:c.147_153del ENSP00000498351.1:p.Lys49AsnfsTer6
ENST00000652572.1:n.251_257del
ENST00000287878.8:c.870_876del ENSP00000287878.3:p.Lys290AsnfsTer6
ENST00000392801.6:c.738_744del ENSP00000376549.2:p.Lys246AsnfsTer6
ENST00000418337.6:c.147_153del ENSP00000387386.2:p.Lys49AsnfsTer6
ENST00000476632.1:c.147_153del ENSP00000419493.1:p.Lys49AsnfsTer6
ENST00000483775.1:n.275_281del
ENST00000488258.5:c.*110_*116del ENSP00000420783.1:n.*110_*116del
ENST00000491938.5:n.216_222del
ENST00000492843.5:c.498_504del ENSP00000419577.1:p.Lys166AsnfsTer6
ENST00000493872.5:c.*119_*125del ENSP00000417252.1:n.*119_*125del
NM_001040633.1:c.738_744del NP_001035723.1:p.Lys246AsnfsTer6
NM_001304527.1:c.495_501del NP_001291456.1:p.Lys165AsnfsTer6
NM_001304531.1:c.147_153del NP_001291460.1:p.Lys49AsnfsTer6
NM_016203.3:c.870_876del NP_057287.2:p.Lys290AsnfsTer6
NM_024429.1:c.147_153del NP_077747.1:p.Lys49AsnfsTer6
XM_005250002.2:c.870_876del XP_005250059.1:p.Lys290AsnfsTer6
XM_005250004.2:c.738_744del XP_005250061.1:p.Lys246AsnfsTer6
XM_005250006.3:c.498_504del XP_005250063.1:p.Lys166AsnfsTer6
XM_006716021.2:c.858_864del XP_006716084.1:p.Lys286AsnfsTer6
XM_011516282.1:c.855_861del XP_011514584.1:p.Lys285AsnfsTer6
XM_011516283.1:c.858_864del XP_011514585.1:p.Lys286AsnfsTer6
XM_011516284.1:c.855_861del XP_011514586.1:p.Lys285AsnfsTer6
XM_011516285.1:c.147_153del XP_011514587.1:p.Lys49AsnfsTer6
XM_011516286.1:c.123_129del XP_011514588.1:p.Lys41AsnfsTer6
XM_011516287.1:c.87_93del XP_011514589.1:p.Lys29AsnfsTer6
NM_001363698.1:c.498_504del NP_001350627.1:p.Lys166AsnfsTer6
XM_005250002.4:c.870_876del XP_005250059.1:p.Lys290AsnfsTer6
XM_005250004.4:c.738_744del XP_005250061.1:p.Lys246AsnfsTer6
XM_005250006.5:c.498_504del XP_005250063.1:p.Lys166AsnfsTer6
XM_011516285.2:c.147_153del XP_011514587.1:p.Lys49AsnfsTer6
XM_011516286.2:c.123_129del XP_011514588.1:p.Lys41AsnfsTer6
XM_017012268.2:c.735_741del XP_016867757.1:p.Lys245AsnfsTer6
XM_017012269.1:c.867_873del XP_016867758.1:p.Lys289AsnfsTer6
XM_017012270.1:c.738_744del XP_016867759.1:p.Lys246AsnfsTer6
XM_017012271.2:c.735_741del XP_016867760.1:p.Lys245AsnfsTer6
XM_017012272.1:c.735_741del XP_016867761.1:p.Lys245AsnfsTer6
XM_017012274.2:c.144_150del XP_016867763.1:p.Lys48AsnfsTer6
XM_017012275.2:c.87_93del XP_016867764.1:p.Lys29AsnfsTer6
XM_017012276.2:c.144_150del XP_016867765.1:p.Lys48AsnfsTer6
XM_017012277.2:c.123_129del XP_016867766.1:p.Lys41AsnfsTer6
XM_017012278.1:c.87_93del XP_016867767.1:p.Lys29AsnfsTer6
XM_017012279.2:c.87_93del XP_016867768.1:p.Lys29AsnfsTer6
XM_017012280.2:c.87_93del XP_016867769.1:p.Lys29AsnfsTer6
XM_017012281.2:c.87_93del XP_016867770.1:p.Lys29AsnfsTer6
XM_024446786.1:c.738_744del XP_024302554.1:p.Lys246AsnfsTer6
XM_024446787.1:c.147_153del XP_024302555.1:p.Lys49AsnfsTer6
XM_024446788.1:c.144_150del XP_024302556.1:p.Lys48AsnfsTer6
XM_024446789.1:c.147_153del XP_024302557.1:p.Lys49AsnfsTer6
NM_016203.4:c.870_876del MANE Select NP_057287.2:p.Lys290AsnfsTer6
NM_001040633.2:c.738_744del NP_001035723.1:p.Lys246AsnfsTer6
NM_001304527.2:c.495_501del NP_001291456.1:p.Lys165AsnfsTer6
NM_001304531.2:c.147_153del NP_001291460.1:p.Lys49AsnfsTer6
NM_001363698.2:c.498_504del NP_001350627.1:p.Lys166AsnfsTer6
NM_024429.2:c.147_153del NP_077747.1:p.Lys49AsnfsTer6