Canonical Allele Identifier: CA370070996

Gene: PRKAG2

Linked Data

• MyVariant Identifiers: chr7:g.151262871A>G (hg19) ; chr7:g.151565785A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151565785A>G , CM000669.2:g.151565785A>G	GRCh38
NC_000007.13:g.151262871A>G , CM000669.1:g.151262871A>G	GRCh37
NC_000007.12:g.150893804A>G	NCBI36
NG_007486.1:g.316446T>C
NG_007486.2:g.316447T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478989.7:c.*70T>C	ENSP00000420645.3:n.*70T>C
ENST00000652321.2:c.1331T>C	ENSP00000498886.2:p.Ile444Thr
ENST00000287878.9:c.1334T>C MANE Select	ENSP00000287878.3:p.Ile445Thr
ENST00000476632.2:c.611T>C	ENSP00000419493.2:p.Ile204Thr
ENST00000478989.6:c.435T>C
ENST00000492843.6:c.959T>C	ENSP00000419577.2:p.Ile320Thr
ENST00000650851.1:n.828T>C
ENST00000650858.1:c.551T>C	ENSP00000498384.1:p.Ile184Thr
ENST00000650948.1:n.2263T>C
ENST00000651188.1:c.*447T>C	ENSP00000498557.1:n.*447T>C
ENST00000651303.1:c.*653T>C	ENSP00000498428.1:n.*653T>C
ENST00000651378.1:c.611T>C	ENSP00000499103.1:p.Ile204Thr
ENST00000651764.1:c.1202T>C	ENSP00000498796.1:p.Ile401Thr
ENST00000651836.1:c.1188T>C	ENSP00000499156.1:n.1188T>C
ENST00000651954.1:n.1550T>C
ENST00000652047.1:c.1199T>C	ENSP00000499111.1:p.Ile400Thr
ENST00000652136.1:n.1881T>C
ENST00000652159.1:c.1202T>C	ENSP00000499025.1:p.Ile401Thr
ENST00000652397.1:c.*70T>C	ENSP00000498351.1:n.*70T>C
ENST00000287878.8:c.1334T>C	ENSP00000287878.3:p.Ile445Thr
ENST00000392801.6:c.1202T>C	ENSP00000376549.2:p.Ile401Thr
ENST00000418337.6:c.611T>C	ENSP00000387386.2:p.Ile204Thr
ENST00000478989.5:c.*70T>C	ENSP00000420645.1:n.*70T>C
ENST00000492843.5:c.962T>C	ENSP00000419577.1:p.Ile321Thr
NM_001040633.1:c.1202T>C	NP_001035723.1:p.Ile401Thr
NM_001304527.1:c.959T>C	NP_001291456.1:p.Ile320Thr
NM_001304531.1:c.611T>C	NP_001291460.1:p.Ile204Thr
NM_016203.3:c.1334T>C	NP_057287.2:p.Ile445Thr
NM_024429.1:c.611T>C	NP_077747.1:p.Ile204Thr
XM_005250002.2:c.1334T>C	XP_005250059.1:p.Ile445Thr
XM_005250004.2:c.1202T>C	XP_005250061.1:p.Ile401Thr
XM_005250006.3:c.962T>C	XP_005250063.1:p.Ile321Thr
XM_006716021.2:c.1322T>C	XP_006716084.1:p.Ile441Thr
XM_011516282.1:c.1319T>C	XP_011514584.1:p.Ile440Thr
XM_011516283.1:c.1322T>C	XP_011514585.1:p.Ile441Thr
XM_011516284.1:c.1319T>C	XP_011514586.1:p.Ile440Thr
XM_011516285.1:c.611T>C	XP_011514587.1:p.Ile204Thr
XM_011516286.1:c.587T>C	XP_011514588.1:p.Ile196Thr
XM_011516287.1:c.551T>C	XP_011514589.1:p.Ile184Thr
NM_001363698.1:c.962T>C	NP_001350627.1:p.Ile321Thr
XM_005250002.4:c.1334T>C	XP_005250059.1:p.Ile445Thr
XM_005250004.4:c.1202T>C	XP_005250061.1:p.Ile401Thr
XM_005250006.5:c.962T>C	XP_005250063.1:p.Ile321Thr
XM_011516285.2:c.611T>C	XP_011514587.1:p.Ile204Thr
XM_011516286.2:c.587T>C	XP_011514588.1:p.Ile196Thr
XM_017012268.2:c.1199T>C	XP_016867757.1:p.Ile400Thr
XM_017012269.1:c.1331T>C	XP_016867758.1:p.Ile444Thr
XM_017012270.1:c.1202T>C	XP_016867759.1:p.Ile401Thr
XM_017012271.2:c.1199T>C	XP_016867760.1:p.Ile400Thr
XM_017012272.1:c.1199T>C	XP_016867761.1:p.Ile400Thr
XM_017012274.2:c.608T>C	XP_016867763.1:p.Ile203Thr
XM_017012275.2:c.551T>C	XP_016867764.1:p.Ile184Thr
XM_017012276.2:c.608T>C	XP_016867765.1:p.Ile203Thr
XM_017012277.2:c.587T>C	XP_016867766.1:p.Ile196Thr
XM_017012278.1:c.551T>C	XP_016867767.1:p.Ile184Thr
XM_017012279.2:c.551T>C	XP_016867768.1:p.Ile184Thr
XM_017012280.2:c.551T>C	XP_016867769.1:p.Ile184Thr
XM_017012281.2:c.551T>C	XP_016867770.1:p.Ile184Thr
XM_024446786.1:c.1202T>C	XP_024302554.1:p.Ile401Thr
XM_024446787.1:c.611T>C	XP_024302555.1:p.Ile204Thr
XM_024446788.1:c.608T>C	XP_024302556.1:p.Ile203Thr
XM_024446789.1:c.611T>C	XP_024302557.1:p.Ile204Thr
NM_016203.4:c.1334T>C MANE Select	NP_057287.2:p.Ile445Thr
NM_001040633.2:c.1202T>C	NP_001035723.1:p.Ile401Thr
NM_001304527.2:c.959T>C	NP_001291456.1:p.Ile320Thr
NM_001304531.2:c.611T>C	NP_001291460.1:p.Ile204Thr
NM_001363698.2:c.962T>C	NP_001350627.1:p.Ile321Thr
NM_024429.2:c.611T>C	NP_077747.1:p.Ile204Thr