Canonical Allele Identifier: CA458670180

Gene: PRKAG2

Linked Data

• MyVariant Identifiers: chr7:g.151269753T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151572667T>G , CM000669.2:g.151572667T>G	GRCh38
NC_000007.13:g.151269753T>G , CM000669.1:g.151269753T>G	GRCh37
NC_000007.12:g.150900686T>G	NCBI36
NG_007486.1:g.309564A>C
NG_007486.2:g.309565A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478989.7:c.322A>C	ENSP00000420645.3:p.Arg108=
ENST00000652321.2:c.1045A>C	ENSP00000498886.2:p.Arg349=
ENST00000287878.9:c.1048A>C MANE Select	ENSP00000287878.3:p.Arg350=
ENST00000476632.2:c.325A>C	ENSP00000419493.2:p.Arg109=
ENST00000478989.6:c.108A>C
ENST00000491938.6:n.391A>C
ENST00000492843.6:c.673A>C	ENSP00000419577.2:p.Arg225=
ENST00000650851.1:n.542A>C
ENST00000650858.1:c.265A>C	ENSP00000498384.1:p.Arg89=
ENST00000650948.1:n.1163A>C
ENST00000651188.1:c.*288A>C	ENSP00000498557.1:n.*288A>C
ENST00000651290.1:n.191A>C
ENST00000651303.1:c.*367A>C	ENSP00000498428.1:n.*367A>C
ENST00000651378.1:c.325A>C	ENSP00000499103.1:p.Arg109=
ENST00000651764.1:c.916A>C	ENSP00000498796.1:p.Arg306=
ENST00000651836.1:c.816A>C	ENSP00000499156.1:n.816A>C
ENST00000652047.1:c.913A>C	ENSP00000499111.1:p.Arg305=
ENST00000652136.1:n.781A>C
ENST00000652159.1:c.916A>C	ENSP00000499025.1:p.Arg306=
ENST00000652397.1:c.325A>C	ENSP00000498351.1:p.Arg109=
ENST00000287878.8:c.1048A>C	ENSP00000287878.3:p.Arg350=
ENST00000392801.6:c.916A>C	ENSP00000376549.2:p.Arg306=
ENST00000418337.6:c.325A>C	ENSP00000387386.2:p.Arg109=
ENST00000476632.1:c.325A>C	ENSP00000419493.1:p.Arg109=
ENST00000478989.5:c.100A>C	ENSP00000420645.1:p.Arg34=
ENST00000488258.5:c.*288A>C	ENSP00000420783.1:n.*288A>C
ENST00000491938.5:n.394A>C
ENST00000492843.5:c.676A>C	ENSP00000419577.1:p.Arg226=
ENST00000493872.5:c.*297A>C	ENSP00000417252.1:n.*297A>C
NM_001040633.1:c.916A>C	NP_001035723.1:p.Arg306=
NM_001304527.1:c.673A>C	NP_001291456.1:p.Arg225=
NM_001304531.1:c.325A>C	NP_001291460.1:p.Arg109=
NM_016203.3:c.1048A>C	NP_057287.2:p.Arg350=
NM_024429.1:c.325A>C	NP_077747.1:p.Arg109=
XM_005250002.2:c.1048A>C	XP_005250059.1:p.Arg350=
XM_005250004.2:c.916A>C	XP_005250061.1:p.Arg306=
XM_005250006.3:c.676A>C	XP_005250063.1:p.Arg226=
XM_006716021.2:c.1036A>C	XP_006716084.1:p.Arg346=
XM_011516282.1:c.1033A>C	XP_011514584.1:p.Arg345=
XM_011516283.1:c.1036A>C	XP_011514585.1:p.Arg346=
XM_011516284.1:c.1033A>C	XP_011514586.1:p.Arg345=
XM_011516285.1:c.325A>C	XP_011514587.1:p.Arg109=
XM_011516286.1:c.301A>C	XP_011514588.1:p.Arg101=
XM_011516287.1:c.265A>C	XP_011514589.1:p.Arg89=
NM_001363698.1:c.676A>C	NP_001350627.1:p.Arg226=
XM_005250002.4:c.1048A>C	XP_005250059.1:p.Arg350=
XM_005250004.4:c.916A>C	XP_005250061.1:p.Arg306=
XM_005250006.5:c.676A>C	XP_005250063.1:p.Arg226=
XM_011516285.2:c.325A>C	XP_011514587.1:p.Arg109=
XM_011516286.2:c.301A>C	XP_011514588.1:p.Arg101=
XM_017012268.2:c.913A>C	XP_016867757.1:p.Arg305=
XM_017012269.1:c.1045A>C	XP_016867758.1:p.Arg349=
XM_017012270.1:c.916A>C	XP_016867759.1:p.Arg306=
XM_017012271.2:c.913A>C	XP_016867760.1:p.Arg305=
XM_017012272.1:c.913A>C	XP_016867761.1:p.Arg305=
XM_017012274.2:c.322A>C	XP_016867763.1:p.Arg108=
XM_017012275.2:c.265A>C	XP_016867764.1:p.Arg89=
XM_017012276.2:c.322A>C	XP_016867765.1:p.Arg108=
XM_017012277.2:c.301A>C	XP_016867766.1:p.Arg101=
XM_017012278.1:c.265A>C	XP_016867767.1:p.Arg89=
XM_017012279.2:c.265A>C	XP_016867768.1:p.Arg89=
XM_017012280.2:c.265A>C	XP_016867769.1:p.Arg89=
XM_017012281.2:c.265A>C	XP_016867770.1:p.Arg89=
XM_024446786.1:c.916A>C	XP_024302554.1:p.Arg306=
XM_024446787.1:c.325A>C	XP_024302555.1:p.Arg109=
XM_024446788.1:c.322A>C	XP_024302556.1:p.Arg108=
XM_024446789.1:c.325A>C	XP_024302557.1:p.Arg109=
NM_016203.4:c.1048A>C MANE Select	NP_057287.2:p.Arg350=
NM_001040633.2:c.916A>C	NP_001035723.1:p.Arg306=
NM_001304527.2:c.673A>C	NP_001291456.1:p.Arg225=
NM_001304531.2:c.325A>C	NP_001291460.1:p.Arg109=
NM_001363698.2:c.676A>C	NP_001350627.1:p.Arg226=
NM_024429.2:c.325A>C	NP_077747.1:p.Arg109=