Canonical Allele Identifier: CA370072182
Gene: PRKAG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151572700A>G , CM000669.2:g.151572700A>G GRCh38
NC_000007.13:g.151269786A>G , CM000669.1:g.151269786A>G GRCh37
NC_000007.12:g.150900719A>G NCBI36
NG_007486.1:g.309531T>C
NG_007486.2:g.309532T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478989.7:c.289T>C ENSP00000420645.3:p.Tyr97His
ENST00000652321.2:c.1012T>C ENSP00000498886.2:p.Tyr338His
ENST00000287878.9:c.1015T>C MANE Select ENSP00000287878.3:p.Tyr339His
ENST00000476632.2:c.292T>C ENSP00000419493.2:p.Tyr98His
ENST00000478989.6:c.75T>C
ENST00000491938.6:n.358T>C
ENST00000492843.6:c.640T>C ENSP00000419577.2:p.Tyr214His
ENST00000650851.1:n.509T>C
ENST00000650858.1:c.232T>C ENSP00000498384.1:p.Tyr78His
ENST00000650948.1:n.1130T>C
ENST00000651188.1:c.*255T>C ENSP00000498557.1:n.*255T>C
ENST00000651290.1:n.158T>C
ENST00000651303.1:c.*334T>C ENSP00000498428.1:n.*334T>C
ENST00000651378.1:c.292T>C ENSP00000499103.1:p.Tyr98His
ENST00000651764.1:c.883T>C ENSP00000498796.1:p.Tyr295His
ENST00000651836.1:c.783T>C ENSP00000499156.1:n.783T>C
ENST00000652047.1:c.880T>C ENSP00000499111.1:p.Tyr294His
ENST00000652136.1:n.748T>C
ENST00000652159.1:c.883T>C ENSP00000499025.1:p.Tyr295His
ENST00000652397.1:c.292T>C ENSP00000498351.1:p.Tyr98His
ENST00000287878.8:c.1015T>C ENSP00000287878.3:p.Tyr339His
ENST00000392801.6:c.883T>C ENSP00000376549.2:p.Tyr295His
ENST00000418337.6:c.292T>C ENSP00000387386.2:p.Tyr98His
ENST00000476632.1:c.292T>C ENSP00000419493.1:p.Tyr98His
ENST00000478989.5:c.67T>C ENSP00000420645.1:p.Tyr23His
ENST00000488258.5:c.*255T>C ENSP00000420783.1:n.*255T>C
ENST00000491938.5:n.361T>C
ENST00000492843.5:c.643T>C ENSP00000419577.1:p.Tyr215His
ENST00000493872.5:c.*264T>C ENSP00000417252.1:n.*264T>C
NM_001040633.1:c.883T>C NP_001035723.1:p.Tyr295His
NM_001304527.1:c.640T>C NP_001291456.1:p.Tyr214His
NM_001304531.1:c.292T>C NP_001291460.1:p.Tyr98His
NM_016203.3:c.1015T>C NP_057287.2:p.Tyr339His
NM_024429.1:c.292T>C NP_077747.1:p.Tyr98His
XM_005250002.2:c.1015T>C XP_005250059.1:p.Tyr339His
XM_005250004.2:c.883T>C XP_005250061.1:p.Tyr295His
XM_005250006.3:c.643T>C XP_005250063.1:p.Tyr215His
XM_006716021.2:c.1003T>C XP_006716084.1:p.Tyr335His
XM_011516282.1:c.1000T>C XP_011514584.1:p.Tyr334His
XM_011516283.1:c.1003T>C XP_011514585.1:p.Tyr335His
XM_011516284.1:c.1000T>C XP_011514586.1:p.Tyr334His
XM_011516285.1:c.292T>C XP_011514587.1:p.Tyr98His
XM_011516286.1:c.268T>C XP_011514588.1:p.Tyr90His
XM_011516287.1:c.232T>C XP_011514589.1:p.Tyr78His
NM_001363698.1:c.643T>C NP_001350627.1:p.Tyr215His
XM_005250002.4:c.1015T>C XP_005250059.1:p.Tyr339His
XM_005250004.4:c.883T>C XP_005250061.1:p.Tyr295His
XM_005250006.5:c.643T>C XP_005250063.1:p.Tyr215His
XM_011516285.2:c.292T>C XP_011514587.1:p.Tyr98His
XM_011516286.2:c.268T>C XP_011514588.1:p.Tyr90His
XM_017012268.2:c.880T>C XP_016867757.1:p.Tyr294His
XM_017012269.1:c.1012T>C XP_016867758.1:p.Tyr338His
XM_017012270.1:c.883T>C XP_016867759.1:p.Tyr295His
XM_017012271.2:c.880T>C XP_016867760.1:p.Tyr294His
XM_017012272.1:c.880T>C XP_016867761.1:p.Tyr294His
XM_017012274.2:c.289T>C XP_016867763.1:p.Tyr97His
XM_017012275.2:c.232T>C XP_016867764.1:p.Tyr78His
XM_017012276.2:c.289T>C XP_016867765.1:p.Tyr97His
XM_017012277.2:c.268T>C XP_016867766.1:p.Tyr90His
XM_017012278.1:c.232T>C XP_016867767.1:p.Tyr78His
XM_017012279.2:c.232T>C XP_016867768.1:p.Tyr78His
XM_017012280.2:c.232T>C XP_016867769.1:p.Tyr78His
XM_017012281.2:c.232T>C XP_016867770.1:p.Tyr78His
XM_024446786.1:c.883T>C XP_024302554.1:p.Tyr295His
XM_024446787.1:c.292T>C XP_024302555.1:p.Tyr98His
XM_024446788.1:c.289T>C XP_024302556.1:p.Tyr97His
XM_024446789.1:c.292T>C XP_024302557.1:p.Tyr98His
NM_016203.4:c.1015T>C MANE Select NP_057287.2:p.Tyr339His
NM_001040633.2:c.883T>C NP_001035723.1:p.Tyr295His
NM_001304527.2:c.640T>C NP_001291456.1:p.Tyr214His
NM_001304531.2:c.292T>C NP_001291460.1:p.Tyr98His
NM_001363698.2:c.643T>C NP_001350627.1:p.Tyr215His
NM_024429.2:c.292T>C NP_077747.1:p.Tyr98His