Canonical Allele Identifier: CA370071594

Gene: PRKAG2

Linked Data

• MyVariant Identifiers: chr7:g.151265889G>C (hg19) ; chr7:g.151568803G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151568803G>C , CM000669.2:g.151568803G>C	GRCh38
NC_000007.13:g.151265889G>C , CM000669.1:g.151265889G>C	GRCh37
NC_000007.12:g.150896822G>C	NCBI36
NG_007486.1:g.313428C>G
NG_007486.2:g.313429C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478989.7:c.420C>G	ENSP00000420645.3:p.Ile140Met
ENST00000652321.2:c.1143C>G	ENSP00000498886.2:p.Ile381Met
ENST00000287878.9:c.1146C>G MANE Select	ENSP00000287878.3:p.Ile382Met
ENST00000476632.2:c.423C>G	ENSP00000419493.2:p.Ile141Met
ENST00000478989.6:c.206C>G
ENST00000492843.6:c.771C>G	ENSP00000419577.2:p.Ile257Met
ENST00000650851.1:n.640C>G
ENST00000650858.1:c.363C>G	ENSP00000498384.1:p.Ile121Met
ENST00000650948.1:n.1261C>G
ENST00000651188.1:c.*346+1368C>G	ENSP00000498557.1:n.*346+1368C>G
ENST00000651303.1:c.*465C>G	ENSP00000498428.1:n.*465C>G
ENST00000651378.1:c.423C>G	ENSP00000499103.1:p.Ile141Met
ENST00000651764.1:c.1014C>G	ENSP00000498796.1:p.Ile338Met
ENST00000651836.1:c.914C>G	ENSP00000499156.1:n.914C>G
ENST00000652047.1:c.1011C>G	ENSP00000499111.1:p.Ile337Met
ENST00000652136.1:n.879C>G
ENST00000652159.1:c.1014C>G	ENSP00000499025.1:p.Ile338Met
ENST00000652397.1:c.423C>G	ENSP00000498351.1:p.Ile141Met
ENST00000287878.8:c.1146C>G	ENSP00000287878.3:p.Ile382Met
ENST00000392801.6:c.1014C>G	ENSP00000376549.2:p.Ile338Met
ENST00000418337.6:c.423C>G	ENSP00000387386.2:p.Ile141Met
ENST00000476632.1:c.423C>G	ENSP00000419493.1:p.Ile141Met
ENST00000478989.5:c.198C>G	ENSP00000420645.1:p.Ile66Met
ENST00000488258.5:c.*386C>G	ENSP00000420783.1:n.*386C>G
ENST00000492843.5:c.774C>G	ENSP00000419577.1:p.Ile258Met
NM_001040633.1:c.1014C>G	NP_001035723.1:p.Ile338Met
NM_001304527.1:c.771C>G	NP_001291456.1:p.Ile257Met
NM_001304531.1:c.423C>G	NP_001291460.1:p.Ile141Met
NM_016203.3:c.1146C>G	NP_057287.2:p.Ile382Met
NM_024429.1:c.423C>G	NP_077747.1:p.Ile141Met
XM_005250002.2:c.1146C>G	XP_005250059.1:p.Ile382Met
XM_005250004.2:c.1014C>G	XP_005250061.1:p.Ile338Met
XM_005250006.3:c.774C>G	XP_005250063.1:p.Ile258Met
XM_006716021.2:c.1134C>G	XP_006716084.1:p.Ile378Met
XM_011516282.1:c.1131C>G	XP_011514584.1:p.Ile377Met
XM_011516283.1:c.1134C>G	XP_011514585.1:p.Ile378Met
XM_011516284.1:c.1131C>G	XP_011514586.1:p.Ile377Met
XM_011516285.1:c.423C>G	XP_011514587.1:p.Ile141Met
XM_011516286.1:c.399C>G	XP_011514588.1:p.Ile133Met
XM_011516287.1:c.363C>G	XP_011514589.1:p.Ile121Met
NM_001363698.1:c.774C>G	NP_001350627.1:p.Ile258Met
XM_005250002.4:c.1146C>G	XP_005250059.1:p.Ile382Met
XM_005250004.4:c.1014C>G	XP_005250061.1:p.Ile338Met
XM_005250006.5:c.774C>G	XP_005250063.1:p.Ile258Met
XM_011516285.2:c.423C>G	XP_011514587.1:p.Ile141Met
XM_011516286.2:c.399C>G	XP_011514588.1:p.Ile133Met
XM_017012268.2:c.1011C>G	XP_016867757.1:p.Ile337Met
XM_017012269.1:c.1143C>G	XP_016867758.1:p.Ile381Met
XM_017012270.1:c.1014C>G	XP_016867759.1:p.Ile338Met
XM_017012271.2:c.1011C>G	XP_016867760.1:p.Ile337Met
XM_017012272.1:c.1011C>G	XP_016867761.1:p.Ile337Met
XM_017012274.2:c.420C>G	XP_016867763.1:p.Ile140Met
XM_017012275.2:c.363C>G	XP_016867764.1:p.Ile121Met
XM_017012276.2:c.420C>G	XP_016867765.1:p.Ile140Met
XM_017012277.2:c.399C>G	XP_016867766.1:p.Ile133Met
XM_017012278.1:c.363C>G	XP_016867767.1:p.Ile121Met
XM_017012279.2:c.363C>G	XP_016867768.1:p.Ile121Met
XM_017012280.2:c.363C>G	XP_016867769.1:p.Ile121Met
XM_017012281.2:c.363C>G	XP_016867770.1:p.Ile121Met
XM_024446786.1:c.1014C>G	XP_024302554.1:p.Ile338Met
XM_024446787.1:c.423C>G	XP_024302555.1:p.Ile141Met
XM_024446788.1:c.420C>G	XP_024302556.1:p.Ile140Met
XM_024446789.1:c.423C>G	XP_024302557.1:p.Ile141Met
NM_016203.4:c.1146C>G MANE Select	NP_057287.2:p.Ile382Met
NM_001040633.2:c.1014C>G	NP_001035723.1:p.Ile338Met
NM_001304527.2:c.771C>G	NP_001291456.1:p.Ile257Met
NM_001304531.2:c.423C>G	NP_001291460.1:p.Ile141Met
NM_001363698.2:c.774C>G	NP_001350627.1:p.Ile258Met
NM_024429.2:c.423C>G	NP_077747.1:p.Ile141Met