Canonical Allele Identifier: CA2685703720
Gene: PRKAG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151781334_151781335insTTCCCTGTGCTGCTCTCC , CM000669.2:g.151781334_151781335insTTCCCTGTGCTGCTCTCC GRCh38
NC_000007.13:g.151478420_151478421insTTCCCTGTGCTGCTCTCC , CM000669.1:g.151478420_151478421insTTCCCTGTGCTGCTCTCC GRCh37
NC_000007.12:g.151109353_151109354insTTCCCTGTGCTGCTCTCC NCBI36
NG_007486.1:g.100896_100897insGGAGAGCAGCACAGGGAA
NG_007486.2:g.100897_100898insGGAGAGCAGCACAGGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000652321.2:c.283_284insGGAGAGCAGCACAGGGAA ENSP00000498886.2:p.Pro95delinsArgArgAlaAlaGlnGlyThr
ENST00000287878.9:c.283_284insGGAGAGCAGCACAGGGAA MANE Select ENSP00000287878.3:p.Pro95delinsArgArgAlaAlaGlnGlyThr
ENST00000650858.1:c.-248+33081_-248+33082insGGAGAGCAGCACAGGGAA ENSP00000498384.1:n.-248+33081_-248+33082insGGAGAGCAGCACAGGGA...
ENST00000650948.1:n.398_399insGGAGAGCAGCACAGGGAA
ENST00000651188.1:c.151_152insGGAGAGCAGCACAGGGAA ENSP00000498557.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
ENST00000651303.1:c.151_152insGGAGAGCAGCACAGGGAA ENSP00000498428.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
ENST00000651378.1:c.-258+33081_-258+33082insGGAGAGCAGCACAGGGAA ENSP00000499103.1:n.-258+33081_-258+33082insGGAGAGCAGCACAGGGA...
ENST00000651764.1:c.151_152insGGAGAGCAGCACAGGGAA ENSP00000498796.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
ENST00000651836.1:c.28_29insGGAGAGCAGCACAGGGAA ENSP00000499156.1:p.Pro10delinsArgArgAlaAlaGlnGlyThr
ENST00000652047.1:c.151_152insGGAGAGCAGCACAGGGAA ENSP00000499111.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
ENST00000652136.1:n.19_20insGGAGAGCAGCACAGGGAA
ENST00000652159.1:c.151_152insGGAGAGCAGCACAGGGAA ENSP00000499025.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
ENST00000652321.1:c.283_284insGGAGAGCAGCACAGGGAA ENSP00000498886.1:p.Pro95delinsArgArgAlaAlaGlnGlyThr
ENST00000652707.1:c.151_152insGGAGAGCAGCACAGGGAA ENSP00000498954.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
ENST00000652714.1:n.456_457insGGAGAGCAGCACAGGGAA
ENST00000287878.8:c.283_284insGGAGAGCAGCACAGGGAA ENSP00000287878.3:p.Pro95delinsArgArgAlaAlaGlnGlyThr
ENST00000392801.6:c.151_152insGGAGAGCAGCACAGGGAA ENSP00000376549.2:p.Pro51delinsArgArgAlaAlaGlnGlyThr
ENST00000461529.1:n.302_303insGGAGAGCAGCACAGGGAA
ENST00000481434.5:n.788_789insGGAGAGCAGCACAGGGAA
ENST00000488258.5:c.283_284insGGAGAGCAGCACAGGGAA ENSP00000420783.1:p.Pro95delinsArgArgAlaAlaGlnGlyThr
NM_001040633.1:c.151_152insGGAGAGCAGCACAGGGAA NP_001035723.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
NM_016203.3:c.283_284insGGAGAGCAGCACAGGGAA NP_057287.2:p.Pro95delinsArgArgAlaAlaGlnGlyThr
XM_005250002.2:c.283_284insGGAGAGCAGCACAGGGAA XP_005250059.1:p.Pro95delinsArgArgAlaAlaGlnGlyThr
XM_005250004.2:c.151_152insGGAGAGCAGCACAGGGAA XP_005250061.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
XM_006716021.2:c.271_272insGGAGAGCAGCACAGGGAA XP_006716084.1:p.Pro91delinsArgArgAlaAlaGlnGlyThr
XM_011516282.1:c.271_272insGGAGAGCAGCACAGGGAA XP_011514584.1:p.Pro91delinsArgArgAlaAlaGlnGlyThr
XM_011516283.1:c.271_272insGGAGAGCAGCACAGGGAA XP_011514585.1:p.Pro91delinsArgArgAlaAlaGlnGlyThr
XM_011516284.1:c.271_272insGGAGAGCAGCACAGGGAA XP_011514586.1:p.Pro91delinsArgArgAlaAlaGlnGlyThr
XM_011516287.1:c.-431_-430insGGAGAGCAGCACAGGGAA XP_011514589.1:n.-431_-430insGGAGAGCAGCACAGGGAA
XM_005250002.4:c.283_284insGGAGAGCAGCACAGGGAA XP_005250059.1:p.Pro95delinsArgArgAlaAlaGlnGlyThr
XM_005250004.4:c.151_152insGGAGAGCAGCACAGGGAA XP_005250061.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
XM_017012268.2:c.151_152insGGAGAGCAGCACAGGGAA XP_016867757.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
XM_017012269.1:c.283_284insGGAGAGCAGCACAGGGAA XP_016867758.1:p.Pro95delinsArgArgAlaAlaGlnGlyThr
XM_017012270.1:c.151_152insGGAGAGCAGCACAGGGAA XP_016867759.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
XM_017012271.2:c.151_152insGGAGAGCAGCACAGGGAA XP_016867760.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
XM_017012272.1:c.151_152insGGAGAGCAGCACAGGGAA XP_016867761.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
XM_017012275.2:c.-428_-427insGGAGAGCAGCACAGGGAA XP_016867764.1:n.-428_-427insGGAGAGCAGCACAGGGAA
XM_017012276.2:c.-467_-466insGGAGAGCAGCACAGGGAA XP_016867765.1:n.-467_-466insGGAGAGCAGCACAGGGAA
XM_017012278.1:c.-431_-430insGGAGAGCAGCACAGGGAA XP_016867767.1:n.-431_-430insGGAGAGCAGCACAGGGAA
XM_017012279.2:c.-431_-430insGGAGAGCAGCACAGGGAA XP_016867768.1:n.-431_-430insGGAGAGCAGCACAGGGAA
XM_017012280.2:c.-428_-427insGGAGAGCAGCACAGGGAA XP_016867769.1:n.-428_-427insGGAGAGCAGCACAGGGAA
XM_017012281.2:c.-454_-453insGGAGAGCAGCACAGGGAA XP_016867770.1:n.-454_-453insGGAGAGCAGCACAGGGAA
XM_024446786.1:c.151_152insGGAGAGCAGCACAGGGAA XP_024302554.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr
XM_024446787.1:c.-467_-466insGGAGAGCAGCACAGGGAA XP_024302555.1:n.-467_-466insGGAGAGCAGCACAGGGAA
XM_024446788.1:c.-467_-466insGGAGAGCAGCACAGGGAA XP_024302556.1:n.-467_-466insGGAGAGCAGCACAGGGAA
XM_024446789.1:c.-467_-466insGGAGAGCAGCACAGGGAA XP_024302557.1:n.-467_-466insGGAGAGCAGCACAGGGAA
NM_016203.4:c.283_284insGGAGAGCAGCACAGGGAA MANE Select NP_057287.2:p.Pro95delinsArgArgAlaAlaGlnGlyThr
NM_001040633.2:c.151_152insGGAGAGCAGCACAGGGAA NP_001035723.1:p.Pro51delinsArgArgAlaAlaGlnGlyThr