Canonical Allele Identifier: CA1752827138
Gene: PRKAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151781423G= , CM000669.2:g.151781423G= GRCh38
NC_000007.13:g.151478509G= , CM000669.1:g.151478509G= GRCh37
NC_000007.12:g.151109442G= NCBI36
NG_007486.1:g.100808C=
NG_007486.2:g.100809C=

Transcript Alleles

HGVS Amino-acid change
ENST00000652321.2:c.195C= ENSP00000498886.2:p.Ser65=
ENST00000287878.9:c.195C= MANE Select ENSP00000287878.3:p.Ser65=
ENST00000650858.1:c.-248+32993C= ENSP00000498384.1:n.-248+32993C=
ENST00000650948.1:n.310C=
ENST00000651188.1:c.63C= ENSP00000498557.1:p.Ser21=
ENST00000651303.1:c.63C= ENSP00000498428.1:p.Ser21=
ENST00000651378.1:c.-258+32993C= ENSP00000499103.1:n.-258+32993C=
ENST00000651764.1:c.63C= ENSP00000498796.1:p.Ser21=
ENST00000652047.1:c.63C= ENSP00000499111.1:p.Ser21=
ENST00000652159.1:c.63C= ENSP00000499025.1:p.Ser21=
ENST00000652321.1:c.195C= ENSP00000498886.1:p.Ser65=
ENST00000652707.1:c.63C= ENSP00000498954.1:p.Ser21=
ENST00000652714.1:n.368C=
ENST00000287878.8:c.195C= ENSP00000287878.3:p.Ser65=
ENST00000392801.6:c.63C= ENSP00000376549.2:p.Ser21=
ENST00000461529.1:n.214C=
ENST00000481434.5:n.700C=
ENST00000488258.5:c.195C= ENSP00000420783.1:p.Ser65=
NM_001040633.1:c.63C= NP_001035723.1:p.Ser21=
NM_016203.3:c.195C= NP_057287.2:p.Ser65=
XM_005250002.2:c.195C= XP_005250059.1:p.Ser65=
XM_005250004.2:c.63C= XP_005250061.1:p.Ser21=
XM_006716021.2:c.183C= XP_006716084.1:p.Ser61=
XM_011516282.1:c.183C= XP_011514584.1:p.Ser61=
XM_011516283.1:c.183C= XP_011514585.1:p.Ser61=
XM_011516284.1:c.183C= XP_011514586.1:p.Ser61=
XM_011516287.1:c.-519C= XP_011514589.1:n.-519C=
XM_005250002.4:c.195C= XP_005250059.1:p.Ser65=
XM_005250004.4:c.63C= XP_005250061.1:p.Ser21=
XM_017012268.2:c.63C= XP_016867757.1:p.Ser21=
XM_017012269.1:c.195C= XP_016867758.1:p.Ser65=
XM_017012270.1:c.63C= XP_016867759.1:p.Ser21=
XM_017012271.2:c.63C= XP_016867760.1:p.Ser21=
XM_017012272.1:c.63C= XP_016867761.1:p.Ser21=
XM_017012275.2:c.-516C= XP_016867764.1:n.-516C=
XM_017012276.2:c.-555C= XP_016867765.1:n.-555C=
XM_017012278.1:c.-519C= XP_016867767.1:n.-519C=
XM_017012279.2:c.-519C= XP_016867768.1:n.-519C=
XM_017012280.2:c.-516C= XP_016867769.1:n.-516C=
XM_017012281.2:c.-542C= XP_016867770.1:n.-542C=
XM_024446786.1:c.63C= XP_024302554.1:p.Ser21=
XM_024446787.1:c.-555C= XP_024302555.1:n.-555C=
XM_024446788.1:c.-555C= XP_024302556.1:n.-555C=
XM_024446789.1:c.-555C= XP_024302557.1:n.-555C=
NM_016203.4:c.195C= MANE Select NP_057287.2:p.Ser65=
NM_001040633.2:c.63C= NP_001035723.1:p.Ser21=