Canonical Allele Identifier: CA370187484

Gene: PRKAG2

Linked Data

• gnomAD v4: 7-151675497-T-A
• MyVariant Identifiers: chr7:g.151372583T>A (hg19) ; chr7:g.151675497T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151675497T>A , CM000669.2:g.151675497T>A	GRCh38
NC_000007.13:g.151372583T>A , CM000669.1:g.151372583T>A	GRCh37
NC_000007.12:g.151003516T>A	NCBI36
NG_007486.1:g.206734A>T
NG_007486.2:g.206735A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652321.2:c.607A>T	ENSP00000498886.2:p.Arg203Trp
ENST00000287878.9:c.607A>T MANE Select	ENSP00000287878.3:p.Arg203Trp
ENST00000487375.2:n.484A>T
ENST00000492843.6:c.235A>T	ENSP00000419577.2:p.Arg79Trp
ENST00000650858.1:c.-107A>T	ENSP00000498384.1:n.-107A>T
ENST00000650948.1:n.722A>T
ENST00000651188.1:c.475A>T	ENSP00000498557.1:p.Arg159Trp
ENST00000651303.1:c.475A>T	ENSP00000498428.1:p.Arg159Trp
ENST00000651378.1:c.-117A>T	ENSP00000499103.1:n.-117A>T
ENST00000651764.1:c.475A>T	ENSP00000498796.1:p.Arg159Trp
ENST00000651836.1:c.378A>T	ENSP00000499156.1:n.378A>T
ENST00000652047.1:c.475A>T	ENSP00000499111.1:p.Arg159Trp
ENST00000652136.1:n.343A>T
ENST00000652159.1:c.475A>T	ENSP00000499025.1:p.Arg159Trp
ENST00000652321.1:c.607A>T	ENSP00000498886.1:p.Arg203Trp
ENST00000652707.1:c.475A>T	ENSP00000498954.1:p.Arg159Trp
ENST00000287878.8:c.607A>T	ENSP00000287878.3:p.Arg203Trp
ENST00000392801.6:c.475A>T	ENSP00000376549.2:p.Arg159Trp
ENST00000481434.5:n.1112A>T
ENST00000487375.1:n.484A>T
ENST00000488258.5:c.607A>T	ENSP00000420783.1:p.Arg203Trp
ENST00000492843.5:c.235A>T	ENSP00000419577.1:p.Arg79Trp
NM_001040633.1:c.475A>T	NP_001035723.1:p.Arg159Trp
NM_001304527.1:c.235A>T	NP_001291456.1:p.Arg79Trp
NM_016203.3:c.607A>T	NP_057287.2:p.Arg203Trp
XM_005250002.2:c.607A>T	XP_005250059.1:p.Arg203Trp
XM_005250004.2:c.475A>T	XP_005250061.1:p.Arg159Trp
XM_005250006.3:c.235A>T	XP_005250063.1:p.Arg79Trp
XM_006716021.2:c.595A>T	XP_006716084.1:p.Arg199Trp
XM_011516282.1:c.595A>T	XP_011514584.1:p.Arg199Trp
XM_011516283.1:c.595A>T	XP_011514585.1:p.Arg199Trp
XM_011516284.1:c.595A>T	XP_011514586.1:p.Arg199Trp
XM_011516287.1:c.-107A>T	XP_011514589.1:n.-107A>T
NM_001363698.1:c.235A>T	NP_001350627.1:p.Arg79Trp
XM_005250002.4:c.607A>T	XP_005250059.1:p.Arg203Trp
XM_005250004.4:c.475A>T	XP_005250061.1:p.Arg159Trp
XM_005250006.5:c.235A>T	XP_005250063.1:p.Arg79Trp
XM_017012268.2:c.475A>T	XP_016867757.1:p.Arg159Trp
XM_017012269.1:c.607A>T	XP_016867758.1:p.Arg203Trp
XM_017012270.1:c.475A>T	XP_016867759.1:p.Arg159Trp
XM_017012271.2:c.475A>T	XP_016867760.1:p.Arg159Trp
XM_017012272.1:c.475A>T	XP_016867761.1:p.Arg159Trp
XM_017012275.2:c.-104A>T	XP_016867764.1:n.-104A>T
XM_017012276.2:c.-117A>T	XP_016867765.1:n.-117A>T
XM_017012278.1:c.-107A>T	XP_016867767.1:n.-107A>T
XM_017012279.2:c.-107A>T	XP_016867768.1:n.-107A>T
XM_017012280.2:c.-104A>T	XP_016867769.1:n.-104A>T
XM_017012281.2:c.-104A>T	XP_016867770.1:n.-104A>T
XM_024446786.1:c.475A>T	XP_024302554.1:p.Arg159Trp
XM_024446787.1:c.-117A>T	XP_024302555.1:n.-117A>T
XM_024446788.1:c.-117A>T	XP_024302556.1:n.-117A>T
XM_024446789.1:c.-117A>T	XP_024302557.1:n.-117A>T
NM_016203.4:c.607A>T MANE Select	NP_057287.2:p.Arg203Trp
NM_001040633.2:c.475A>T	NP_001035723.1:p.Arg159Trp
NM_001304527.2:c.235A>T	NP_001291456.1:p.Arg79Trp
NM_001363698.2:c.235A>T	NP_001350627.1:p.Arg79Trp