Canonical Allele Identifier: CA370070477

Gene: PRKAG2

Linked Data

• MyVariant Identifiers: chr7:g.151261189A>G (hg19) ; chr7:g.151564103A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151564103A>G , CM000669.2:g.151564103A>G	GRCh38
NC_000007.13:g.151261189A>G , CM000669.1:g.151261189A>G	GRCh37
NC_000007.12:g.150892122A>G	NCBI36
NG_007486.1:g.318128T>C
NG_007486.2:g.318129T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478989.7:c.*295T>C	ENSP00000420645.3:n.*295T>C
ENST00000652321.2:c.1556T>C	ENSP00000498886.2:p.Ile519Thr
ENST00000287878.9:c.1559T>C MANE Select	ENSP00000287878.3:p.Ile520Thr
ENST00000476632.2:c.836T>C	ENSP00000419493.2:p.Ile279Thr
ENST00000492843.6:c.1184T>C	ENSP00000419577.2:p.Ile395Thr
ENST00000650851.1:n.1053T>C
ENST00000650858.1:c.776T>C	ENSP00000498384.1:p.Ile259Thr
ENST00000650948.1:n.3945T>C
ENST00000651188.1:c.*672T>C	ENSP00000498557.1:n.*672T>C
ENST00000651303.1:c.*878T>C	ENSP00000498428.1:n.*878T>C
ENST00000651378.1:c.836T>C	ENSP00000499103.1:p.Ile279Thr
ENST00000651764.1:c.1427T>C	ENSP00000498796.1:p.Ile476Thr
ENST00000651836.1:c.1749T>C	ENSP00000499156.1:n.1749T>C
ENST00000651954.1:n.1775T>C
ENST00000652047.1:c.1424T>C	ENSP00000499111.1:p.Ile475Thr
ENST00000652136.1:n.2106T>C
ENST00000652159.1:c.1427T>C	ENSP00000499025.1:p.Ile476Thr
ENST00000652397.1:c.*295T>C	ENSP00000498351.1:n.*295T>C
ENST00000287878.8:c.1559T>C	ENSP00000287878.3:p.Ile520Thr
ENST00000392801.6:c.1427T>C	ENSP00000376549.2:p.Ile476Thr
ENST00000418337.6:c.836T>C	ENSP00000387386.2:p.Ile279Thr
ENST00000479461.1:n.211T>C
ENST00000485183.1:n.212T>C
ENST00000492843.5:c.1187T>C	ENSP00000419577.1:p.Ile396Thr
NM_001040633.1:c.1427T>C	NP_001035723.1:p.Ile476Thr
NM_001304527.1:c.1184T>C	NP_001291456.1:p.Ile395Thr
NM_001304531.1:c.836T>C	NP_001291460.1:p.Ile279Thr
NM_016203.3:c.1559T>C	NP_057287.2:p.Ile520Thr
NM_024429.1:c.836T>C	NP_077747.1:p.Ile279Thr
XM_005250002.2:c.1559T>C	XP_005250059.1:p.Ile520Thr
XM_005250004.2:c.1427T>C	XP_005250061.1:p.Ile476Thr
XM_005250006.3:c.1187T>C	XP_005250063.1:p.Ile396Thr
XM_006716021.2:c.1547T>C	XP_006716084.1:p.Ile516Thr
XM_011516282.1:c.1544T>C	XP_011514584.1:p.Ile515Thr
XM_011516283.1:c.1547T>C	XP_011514585.1:p.Ile516Thr
XM_011516284.1:c.1544T>C	XP_011514586.1:p.Ile515Thr
XM_011516285.1:c.836T>C	XP_011514587.1:p.Ile279Thr
XM_011516286.1:c.812T>C	XP_011514588.1:p.Ile271Thr
XM_011516287.1:c.776T>C	XP_011514589.1:p.Ile259Thr
NM_001363698.1:c.1187T>C	NP_001350627.1:p.Ile396Thr
XM_005250002.4:c.1559T>C	XP_005250059.1:p.Ile520Thr
XM_005250004.4:c.1427T>C	XP_005250061.1:p.Ile476Thr
XM_005250006.5:c.1187T>C	XP_005250063.1:p.Ile396Thr
XM_011516285.2:c.836T>C	XP_011514587.1:p.Ile279Thr
XM_011516286.2:c.812T>C	XP_011514588.1:p.Ile271Thr
XM_017012268.2:c.1424T>C	XP_016867757.1:p.Ile475Thr
XM_017012269.1:c.1556T>C	XP_016867758.1:p.Ile519Thr
XM_017012270.1:c.1427T>C	XP_016867759.1:p.Ile476Thr
XM_017012271.2:c.1424T>C	XP_016867760.1:p.Ile475Thr
XM_017012272.1:c.1424T>C	XP_016867761.1:p.Ile475Thr
XM_017012274.2:c.833T>C	XP_016867763.1:p.Ile278Thr
XM_017012275.2:c.776T>C	XP_016867764.1:p.Ile259Thr
XM_017012276.2:c.833T>C	XP_016867765.1:p.Ile278Thr
XM_017012277.2:c.812T>C	XP_016867766.1:p.Ile271Thr
XM_017012278.1:c.776T>C	XP_016867767.1:p.Ile259Thr
XM_017012279.2:c.776T>C	XP_016867768.1:p.Ile259Thr
XM_017012280.2:c.776T>C	XP_016867769.1:p.Ile259Thr
XM_017012281.2:c.776T>C	XP_016867770.1:p.Ile259Thr
XM_024446786.1:c.1427T>C	XP_024302554.1:p.Ile476Thr
XM_024446787.1:c.836T>C	XP_024302555.1:p.Ile279Thr
XM_024446788.1:c.833T>C	XP_024302556.1:p.Ile278Thr
XM_024446789.1:c.836T>C	XP_024302557.1:p.Ile279Thr
NM_016203.4:c.1559T>C MANE Select	NP_057287.2:p.Ile520Thr
NM_001040633.2:c.1427T>C	NP_001035723.1:p.Ile476Thr
NM_001304527.2:c.1184T>C	NP_001291456.1:p.Ile395Thr
NM_001304531.2:c.836T>C	NP_001291460.1:p.Ile279Thr
NM_001363698.2:c.1187T>C	NP_001350627.1:p.Ile396Thr
NM_024429.2:c.836T>C	NP_077747.1:p.Ile279Thr