Canonical Allele Identifier: CA056900
Gene: PRKAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 487637
dbSNP Id: rs775756069

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151781259C>T , CM000669.2:g.151781259C>T GRCh38
NC_000007.13:g.151478345C>T , CM000669.1:g.151478345C>T GRCh37
NC_000007.12:g.151109278C>T NCBI36
NG_007486.1:g.100972G>A
NG_007486.2:g.100973G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652321.2:c.359G>A ENSP00000498886.2:p.Arg120His
ENST00000287878.9:c.359G>A MANE Select ENSP00000287878.3:p.Arg120His
ENST00000650858.1:c.-248+33157G>A ENSP00000498384.1:n.-248+33157G>A
ENST00000650948.1:n.474G>A
ENST00000651188.1:c.227G>A ENSP00000498557.1:p.Arg76His
ENST00000651303.1:c.227G>A ENSP00000498428.1:p.Arg76His
ENST00000651378.1:c.-258+33157G>A ENSP00000499103.1:n.-258+33157G>A
ENST00000651764.1:c.227G>A ENSP00000498796.1:p.Arg76His
ENST00000651836.1:c.104G>A ENSP00000499156.1:p.Arg35His
ENST00000652047.1:c.227G>A ENSP00000499111.1:p.Arg76His
ENST00000652136.1:n.95G>A
ENST00000652159.1:c.227G>A ENSP00000499025.1:p.Arg76His
ENST00000652321.1:c.359G>A ENSP00000498886.1:p.Arg120His
ENST00000652707.1:c.227G>A ENSP00000498954.1:p.Arg76His
ENST00000652714.1:n.532G>A
ENST00000287878.8:c.359G>A ENSP00000287878.3:p.Arg120His
ENST00000392801.6:c.227G>A ENSP00000376549.2:p.Arg76His
ENST00000461529.1:n.378G>A
ENST00000481434.5:n.864G>A
ENST00000488258.5:c.359G>A ENSP00000420783.1:p.Arg120His
NM_001040633.1:c.227G>A NP_001035723.1:p.Arg76His
NM_016203.3:c.359G>A NP_057287.2:p.Arg120His
XM_005250002.2:c.359G>A XP_005250059.1:p.Arg120His
XM_005250004.2:c.227G>A XP_005250061.1:p.Arg76His
XM_006716021.2:c.347G>A XP_006716084.1:p.Arg116His
XM_011516282.1:c.347G>A XP_011514584.1:p.Arg116His
XM_011516283.1:c.347G>A XP_011514585.1:p.Arg116His
XM_011516284.1:c.347G>A XP_011514586.1:p.Arg116His
XM_011516287.1:c.-355G>A XP_011514589.1:n.-355G>A
XM_005250002.4:c.359G>A XP_005250059.1:p.Arg120His
XM_005250004.4:c.227G>A XP_005250061.1:p.Arg76His
XM_017012268.2:c.227G>A XP_016867757.1:p.Arg76His
XM_017012269.1:c.359G>A XP_016867758.1:p.Arg120His
XM_017012270.1:c.227G>A XP_016867759.1:p.Arg76His
XM_017012271.2:c.227G>A XP_016867760.1:p.Arg76His
XM_017012272.1:c.227G>A XP_016867761.1:p.Arg76His
XM_017012275.2:c.-352G>A XP_016867764.1:n.-352G>A
XM_017012276.2:c.-391G>A XP_016867765.1:n.-391G>A
XM_017012278.1:c.-355G>A XP_016867767.1:n.-355G>A
XM_017012279.2:c.-355G>A XP_016867768.1:n.-355G>A
XM_017012280.2:c.-352G>A XP_016867769.1:n.-352G>A
XM_017012281.2:c.-378G>A XP_016867770.1:n.-378G>A
XM_024446786.1:c.227G>A XP_024302554.1:p.Arg76His
XM_024446787.1:c.-391G>A XP_024302555.1:n.-391G>A
XM_024446788.1:c.-391G>A XP_024302556.1:n.-391G>A
XM_024446789.1:c.-391G>A XP_024302557.1:n.-391G>A
NM_016203.4:c.359G>A MANE Select NP_057287.2:p.Arg120His
NM_001040633.2:c.227G>A NP_001035723.1:p.Arg76His