Canonical Allele Identifier: CA370186920

Gene: PRKAG2

Linked Data

• ClinVar Variation Id: 533874
• ClinVar RCV Id: RCV000641179
• dbSNP Id: rs1289045435
• MyVariant Identifiers: chr7:g.151372525T>C (hg19) ; chr7:g.151675439T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151675439T>C , CM000669.2:g.151675439T>C	GRCh38
NC_000007.13:g.151372525T>C , CM000669.1:g.151372525T>C	GRCh37
NC_000007.12:g.151003458T>C	NCBI36
NG_007486.1:g.206792A>G
NG_007486.2:g.206793A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652321.2:c.665A>G	ENSP00000498886.2:p.His222Arg
ENST00000287878.9:c.665A>G MANE Select	ENSP00000287878.3:p.His222Arg
ENST00000487375.2:n.542A>G
ENST00000492843.6:c.293A>G	ENSP00000419577.2:p.His98Arg
ENST00000650858.1:c.-49A>G	ENSP00000498384.1:n.-49A>G
ENST00000650948.1:n.780A>G
ENST00000651188.1:c.533A>G	ENSP00000498557.1:p.His178Arg
ENST00000651303.1:c.533A>G	ENSP00000498428.1:p.His178Arg
ENST00000651378.1:c.-59A>G	ENSP00000499103.1:n.-59A>G
ENST00000651764.1:c.533A>G	ENSP00000498796.1:p.His178Arg
ENST00000651836.1:c.436A>G	ENSP00000499156.1:n.436A>G
ENST00000652047.1:c.533A>G	ENSP00000499111.1:p.His178Arg
ENST00000652136.1:n.401A>G
ENST00000652159.1:c.533A>G	ENSP00000499025.1:p.His178Arg
ENST00000652321.1:c.665A>G	ENSP00000498886.1:p.His222Arg
ENST00000652707.1:c.533A>G	ENSP00000498954.1:p.His178Arg
ENST00000287878.8:c.665A>G	ENSP00000287878.3:p.His222Arg
ENST00000392801.6:c.533A>G	ENSP00000376549.2:p.His178Arg
ENST00000481434.5:n.1170A>G
ENST00000487375.1:n.542A>G
ENST00000488258.5:c.665A>G	ENSP00000420783.1:p.His222Arg
ENST00000492843.5:c.293A>G	ENSP00000419577.1:p.His98Arg
NM_001040633.1:c.533A>G	NP_001035723.1:p.His178Arg
NM_001304527.1:c.293A>G	NP_001291456.1:p.His98Arg
NM_016203.3:c.665A>G	NP_057287.2:p.His222Arg
XM_005250002.2:c.665A>G	XP_005250059.1:p.His222Arg
XM_005250004.2:c.533A>G	XP_005250061.1:p.His178Arg
XM_005250006.3:c.293A>G	XP_005250063.1:p.His98Arg
XM_006716021.2:c.653A>G	XP_006716084.1:p.His218Arg
XM_011516282.1:c.653A>G	XP_011514584.1:p.His218Arg
XM_011516283.1:c.653A>G	XP_011514585.1:p.His218Arg
XM_011516284.1:c.653A>G	XP_011514586.1:p.His218Arg
XM_011516287.1:c.-49A>G	XP_011514589.1:n.-49A>G
NM_001363698.1:c.293A>G	NP_001350627.1:p.His98Arg
XM_005250002.4:c.665A>G	XP_005250059.1:p.His222Arg
XM_005250004.4:c.533A>G	XP_005250061.1:p.His178Arg
XM_005250006.5:c.293A>G	XP_005250063.1:p.His98Arg
XM_017012268.2:c.533A>G	XP_016867757.1:p.His178Arg
XM_017012269.1:c.665A>G	XP_016867758.1:p.His222Arg
XM_017012270.1:c.533A>G	XP_016867759.1:p.His178Arg
XM_017012271.2:c.533A>G	XP_016867760.1:p.His178Arg
XM_017012272.1:c.533A>G	XP_016867761.1:p.His178Arg
XM_017012275.2:c.-46A>G	XP_016867764.1:n.-46A>G
XM_017012276.2:c.-59A>G	XP_016867765.1:n.-59A>G
XM_017012278.1:c.-49A>G	XP_016867767.1:n.-49A>G
XM_017012279.2:c.-49A>G	XP_016867768.1:n.-49A>G
XM_017012280.2:c.-46A>G	XP_016867769.1:n.-46A>G
XM_017012281.2:c.-46A>G	XP_016867770.1:n.-46A>G
XM_024446786.1:c.533A>G	XP_024302554.1:p.His178Arg
XM_024446787.1:c.-59A>G	XP_024302555.1:n.-59A>G
XM_024446788.1:c.-59A>G	XP_024302556.1:n.-59A>G
XM_024446789.1:c.-59A>G	XP_024302557.1:n.-59A>G
NM_016203.4:c.665A>G MANE Select	NP_057287.2:p.His222Arg
NM_001040633.2:c.533A>G	NP_001035723.1:p.His178Arg
NM_001304527.2:c.293A>G	NP_001291456.1:p.His98Arg
NM_001363698.2:c.293A>G	NP_001350627.1:p.His98Arg