Canonical Allele Identifier: CA370071664

Gene: PRKAG2

Linked Data

• MyVariant Identifiers: chr7:g.151265918C>T (hg19) ; chr7:g.151568832C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151568832C>T , CM000669.2:g.151568832C>T	GRCh38
NC_000007.13:g.151265918C>T , CM000669.1:g.151265918C>T	GRCh37
NC_000007.12:g.150896851C>T	NCBI36
NG_007486.1:g.313399G>A
NG_007486.2:g.313400G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478989.7:c.391G>A	ENSP00000420645.3:p.Ala131Thr
ENST00000652321.2:c.1114G>A	ENSP00000498886.2:p.Ala372Thr
ENST00000287878.9:c.1117G>A MANE Select	ENSP00000287878.3:p.Ala373Thr
ENST00000476632.2:c.394G>A	ENSP00000419493.2:p.Ala132Thr
ENST00000478989.6:c.177G>A
ENST00000492843.6:c.742G>A	ENSP00000419577.2:p.Ala248Thr
ENST00000650851.1:n.611G>A
ENST00000650858.1:c.334G>A	ENSP00000498384.1:p.Ala112Thr
ENST00000650948.1:n.1232G>A
ENST00000651188.1:c.*346+1339G>A	ENSP00000498557.1:n.*346+1339G>A
ENST00000651303.1:c.*436G>A	ENSP00000498428.1:n.*436G>A
ENST00000651378.1:c.394G>A	ENSP00000499103.1:p.Ala132Thr
ENST00000651764.1:c.985G>A	ENSP00000498796.1:p.Ala329Thr
ENST00000651836.1:c.885G>A	ENSP00000499156.1:n.885G>A
ENST00000652047.1:c.982G>A	ENSP00000499111.1:p.Ala328Thr
ENST00000652136.1:n.850G>A
ENST00000652159.1:c.985G>A	ENSP00000499025.1:p.Ala329Thr
ENST00000652397.1:c.394G>A	ENSP00000498351.1:p.Ala132Thr
ENST00000287878.8:c.1117G>A	ENSP00000287878.3:p.Ala373Thr
ENST00000392801.6:c.985G>A	ENSP00000376549.2:p.Ala329Thr
ENST00000418337.6:c.394G>A	ENSP00000387386.2:p.Ala132Thr
ENST00000476632.1:c.394G>A	ENSP00000419493.1:p.Ala132Thr
ENST00000478989.5:c.169G>A	ENSP00000420645.1:p.Ala57Thr
ENST00000488258.5:c.*357G>A	ENSP00000420783.1:n.*357G>A
ENST00000492843.5:c.745G>A	ENSP00000419577.1:p.Ala249Thr
NM_001040633.1:c.985G>A	NP_001035723.1:p.Ala329Thr
NM_001304527.1:c.742G>A	NP_001291456.1:p.Ala248Thr
NM_001304531.1:c.394G>A	NP_001291460.1:p.Ala132Thr
NM_016203.3:c.1117G>A	NP_057287.2:p.Ala373Thr
NM_024429.1:c.394G>A	NP_077747.1:p.Ala132Thr
XM_005250002.2:c.1117G>A	XP_005250059.1:p.Ala373Thr
XM_005250004.2:c.985G>A	XP_005250061.1:p.Ala329Thr
XM_005250006.3:c.745G>A	XP_005250063.1:p.Ala249Thr
XM_006716021.2:c.1105G>A	XP_006716084.1:p.Ala369Thr
XM_011516282.1:c.1102G>A	XP_011514584.1:p.Ala368Thr
XM_011516283.1:c.1105G>A	XP_011514585.1:p.Ala369Thr
XM_011516284.1:c.1102G>A	XP_011514586.1:p.Ala368Thr
XM_011516285.1:c.394G>A	XP_011514587.1:p.Ala132Thr
XM_011516286.1:c.370G>A	XP_011514588.1:p.Ala124Thr
XM_011516287.1:c.334G>A	XP_011514589.1:p.Ala112Thr
NM_001363698.1:c.745G>A	NP_001350627.1:p.Ala249Thr
XM_005250002.4:c.1117G>A	XP_005250059.1:p.Ala373Thr
XM_005250004.4:c.985G>A	XP_005250061.1:p.Ala329Thr
XM_005250006.5:c.745G>A	XP_005250063.1:p.Ala249Thr
XM_011516285.2:c.394G>A	XP_011514587.1:p.Ala132Thr
XM_011516286.2:c.370G>A	XP_011514588.1:p.Ala124Thr
XM_017012268.2:c.982G>A	XP_016867757.1:p.Ala328Thr
XM_017012269.1:c.1114G>A	XP_016867758.1:p.Ala372Thr
XM_017012270.1:c.985G>A	XP_016867759.1:p.Ala329Thr
XM_017012271.2:c.982G>A	XP_016867760.1:p.Ala328Thr
XM_017012272.1:c.982G>A	XP_016867761.1:p.Ala328Thr
XM_017012274.2:c.391G>A	XP_016867763.1:p.Ala131Thr
XM_017012275.2:c.334G>A	XP_016867764.1:p.Ala112Thr
XM_017012276.2:c.391G>A	XP_016867765.1:p.Ala131Thr
XM_017012277.2:c.370G>A	XP_016867766.1:p.Ala124Thr
XM_017012278.1:c.334G>A	XP_016867767.1:p.Ala112Thr
XM_017012279.2:c.334G>A	XP_016867768.1:p.Ala112Thr
XM_017012280.2:c.334G>A	XP_016867769.1:p.Ala112Thr
XM_017012281.2:c.334G>A	XP_016867770.1:p.Ala112Thr
XM_024446786.1:c.985G>A	XP_024302554.1:p.Ala329Thr
XM_024446787.1:c.394G>A	XP_024302555.1:p.Ala132Thr
XM_024446788.1:c.391G>A	XP_024302556.1:p.Ala131Thr
XM_024446789.1:c.394G>A	XP_024302557.1:p.Ala132Thr
NM_016203.4:c.1117G>A MANE Select	NP_057287.2:p.Ala373Thr
NM_001040633.2:c.985G>A	NP_001035723.1:p.Ala329Thr
NM_001304527.2:c.742G>A	NP_001291456.1:p.Ala248Thr
NM_001304531.2:c.394G>A	NP_001291460.1:p.Ala132Thr
NM_001363698.2:c.745G>A	NP_001350627.1:p.Ala249Thr
NM_024429.2:c.394G>A	NP_077747.1:p.Ala132Thr