Canonical Allele Identifier: CA370070593

Gene: PRKAG2

Linked Data

• MyVariant Identifiers: chr7:g.151261241G>A (hg19) ; chr7:g.151564155G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151564155G>A , CM000669.2:g.151564155G>A	GRCh38
NC_000007.13:g.151261241G>A , CM000669.1:g.151261241G>A	GRCh37
NC_000007.12:g.150892174G>A	NCBI36
NG_007486.1:g.318076C>T
NG_007486.2:g.318077C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478989.7:c.*243C>T	ENSP00000420645.3:n.*243C>T
ENST00000652321.2:c.1504C>T	ENSP00000498886.2:p.Gln502Ter
ENST00000287878.9:c.1507C>T MANE Select	ENSP00000287878.3:p.Gln503Ter
ENST00000476632.2:c.784C>T	ENSP00000419493.2:p.Gln262Ter
ENST00000492843.6:c.1132C>T	ENSP00000419577.2:p.Gln378Ter
ENST00000650851.1:n.1001C>T
ENST00000650858.1:c.724C>T	ENSP00000498384.1:p.Gln242Ter
ENST00000650948.1:n.3893C>T
ENST00000651188.1:c.*620C>T	ENSP00000498557.1:n.*620C>T
ENST00000651303.1:c.*826C>T	ENSP00000498428.1:n.*826C>T
ENST00000651378.1:c.784C>T	ENSP00000499103.1:p.Gln262Ter
ENST00000651764.1:c.1375C>T	ENSP00000498796.1:p.Gln459Ter
ENST00000651836.1:c.1697C>T	ENSP00000499156.1:n.1697C>T
ENST00000651954.1:n.1723C>T
ENST00000652047.1:c.1372C>T	ENSP00000499111.1:p.Gln458Ter
ENST00000652136.1:n.2054C>T
ENST00000652159.1:c.1375C>T	ENSP00000499025.1:p.Gln459Ter
ENST00000652397.1:c.*243C>T	ENSP00000498351.1:n.*243C>T
ENST00000287878.8:c.1507C>T	ENSP00000287878.3:p.Gln503Ter
ENST00000392801.6:c.1375C>T	ENSP00000376549.2:p.Gln459Ter
ENST00000418337.6:c.784C>T	ENSP00000387386.2:p.Gln262Ter
ENST00000479461.1:n.159C>T
ENST00000485183.1:n.160C>T
ENST00000492843.5:c.1135C>T	ENSP00000419577.1:p.Gln379Ter
NM_001040633.1:c.1375C>T	NP_001035723.1:p.Gln459Ter
NM_001304527.1:c.1132C>T	NP_001291456.1:p.Gln378Ter
NM_001304531.1:c.784C>T	NP_001291460.1:p.Gln262Ter
NM_016203.3:c.1507C>T	NP_057287.2:p.Gln503Ter
NM_024429.1:c.784C>T	NP_077747.1:p.Gln262Ter
XM_005250002.2:c.1507C>T	XP_005250059.1:p.Gln503Ter
XM_005250004.2:c.1375C>T	XP_005250061.1:p.Gln459Ter
XM_005250006.3:c.1135C>T	XP_005250063.1:p.Gln379Ter
XM_006716021.2:c.1495C>T	XP_006716084.1:p.Gln499Ter
XM_011516282.1:c.1492C>T	XP_011514584.1:p.Gln498Ter
XM_011516283.1:c.1495C>T	XP_011514585.1:p.Gln499Ter
XM_011516284.1:c.1492C>T	XP_011514586.1:p.Gln498Ter
XM_011516285.1:c.784C>T	XP_011514587.1:p.Gln262Ter
XM_011516286.1:c.760C>T	XP_011514588.1:p.Gln254Ter
XM_011516287.1:c.724C>T	XP_011514589.1:p.Gln242Ter
NM_001363698.1:c.1135C>T	NP_001350627.1:p.Gln379Ter
XM_005250002.4:c.1507C>T	XP_005250059.1:p.Gln503Ter
XM_005250004.4:c.1375C>T	XP_005250061.1:p.Gln459Ter
XM_005250006.5:c.1135C>T	XP_005250063.1:p.Gln379Ter
XM_011516285.2:c.784C>T	XP_011514587.1:p.Gln262Ter
XM_011516286.2:c.760C>T	XP_011514588.1:p.Gln254Ter
XM_017012268.2:c.1372C>T	XP_016867757.1:p.Gln458Ter
XM_017012269.1:c.1504C>T	XP_016867758.1:p.Gln502Ter
XM_017012270.1:c.1375C>T	XP_016867759.1:p.Gln459Ter
XM_017012271.2:c.1372C>T	XP_016867760.1:p.Gln458Ter
XM_017012272.1:c.1372C>T	XP_016867761.1:p.Gln458Ter
XM_017012274.2:c.781C>T	XP_016867763.1:p.Gln261Ter
XM_017012275.2:c.724C>T	XP_016867764.1:p.Gln242Ter
XM_017012276.2:c.781C>T	XP_016867765.1:p.Gln261Ter
XM_017012277.2:c.760C>T	XP_016867766.1:p.Gln254Ter
XM_017012278.1:c.724C>T	XP_016867767.1:p.Gln242Ter
XM_017012279.2:c.724C>T	XP_016867768.1:p.Gln242Ter
XM_017012280.2:c.724C>T	XP_016867769.1:p.Gln242Ter
XM_017012281.2:c.724C>T	XP_016867770.1:p.Gln242Ter
XM_024446786.1:c.1375C>T	XP_024302554.1:p.Gln459Ter
XM_024446787.1:c.784C>T	XP_024302555.1:p.Gln262Ter
XM_024446788.1:c.781C>T	XP_024302556.1:p.Gln261Ter
XM_024446789.1:c.784C>T	XP_024302557.1:p.Gln262Ter
NM_016203.4:c.1507C>T MANE Select	NP_057287.2:p.Gln503Ter
NM_001040633.2:c.1375C>T	NP_001035723.1:p.Gln459Ter
NM_001304527.2:c.1132C>T	NP_001291456.1:p.Gln378Ter
NM_001304531.2:c.784C>T	NP_001291460.1:p.Gln262Ter
NM_001363698.2:c.1135C>T	NP_001350627.1:p.Gln379Ter
NM_024429.2:c.784C>T	NP_077747.1:p.Gln262Ter