Canonical Allele Identifier: CA1752827127

Gene: PRKAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151781419_151781420delinsAG , CM000669.2:g.151781419_151781420delinsAG	GRCh38
NC_000007.13:g.151478505_151478506delinsAG , CM000669.1:g.151478505_151478506delinsAG	GRCh37
NC_000007.12:g.151109438_151109439delinsAG	NCBI36
NG_007486.1:g.100811_100812delinsCT
NG_007486.2:g.100812_100813delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652321.2:c.198_199delinsCT	ENSP00000498886.2:p.Pro66=
ENST00000287878.9:c.198_199delinsCT MANE Select	ENSP00000287878.3:p.Pro66=
ENST00000650858.1:c.-248+32996_-248+32997delinsCT	ENSP00000498384.1:n.-248+32996_-248+32997delinsCT
ENST00000650948.1:n.313_314delinsCT
ENST00000651188.1:c.66_67delinsCT	ENSP00000498557.1:p.Pro22=
ENST00000651303.1:c.66_67delinsCT	ENSP00000498428.1:p.Pro22=
ENST00000651378.1:c.-258+32996_-258+32997delinsCT	ENSP00000499103.1:n.-258+32996_-258+32997delinsCT
ENST00000651764.1:c.66_67delinsCT	ENSP00000498796.1:p.Pro22=
ENST00000652047.1:c.66_67delinsCT	ENSP00000499111.1:p.Pro22=
ENST00000652159.1:c.66_67delinsCT	ENSP00000499025.1:p.Pro22=
ENST00000652321.1:c.198_199delinsCT	ENSP00000498886.1:p.Pro66=
ENST00000652707.1:c.66_67delinsCT	ENSP00000498954.1:p.Pro22=
ENST00000652714.1:n.371_372delinsCT
ENST00000287878.8:c.198_199delinsCT	ENSP00000287878.3:p.Pro66=
ENST00000392801.6:c.66_67delinsCT	ENSP00000376549.2:p.Pro22=
ENST00000461529.1:n.217_218delinsCT
ENST00000481434.5:n.703_704delinsCT
ENST00000488258.5:c.198_199delinsCT	ENSP00000420783.1:p.Pro66=
NM_001040633.1:c.66_67delinsCT	NP_001035723.1:p.Pro22=
NM_016203.3:c.198_199delinsCT	NP_057287.2:p.Pro66=
XM_005250002.2:c.198_199delinsCT	XP_005250059.1:p.Pro66=
XM_005250004.2:c.66_67delinsCT	XP_005250061.1:p.Pro22=
XM_006716021.2:c.186_187delinsCT	XP_006716084.1:p.Pro62=
XM_011516282.1:c.186_187delinsCT	XP_011514584.1:p.Pro62=
XM_011516283.1:c.186_187delinsCT	XP_011514585.1:p.Pro62=
XM_011516284.1:c.186_187delinsCT	XP_011514586.1:p.Pro62=
XM_011516287.1:c.-516_-515delinsCT	XP_011514589.1:n.-516_-515delinsCT
XM_005250002.4:c.198_199delinsCT	XP_005250059.1:p.Pro66=
XM_005250004.4:c.66_67delinsCT	XP_005250061.1:p.Pro22=
XM_017012268.2:c.66_67delinsCT	XP_016867757.1:p.Pro22=
XM_017012269.1:c.198_199delinsCT	XP_016867758.1:p.Pro66=
XM_017012270.1:c.66_67delinsCT	XP_016867759.1:p.Pro22=
XM_017012271.2:c.66_67delinsCT	XP_016867760.1:p.Pro22=
XM_017012272.1:c.66_67delinsCT	XP_016867761.1:p.Pro22=
XM_017012275.2:c.-513_-512delinsCT	XP_016867764.1:n.-513_-512delinsCT
XM_017012276.2:c.-552_-551delinsCT	XP_016867765.1:n.-552_-551delinsCT
XM_017012278.1:c.-516_-515delinsCT	XP_016867767.1:n.-516_-515delinsCT
XM_017012279.2:c.-516_-515delinsCT	XP_016867768.1:n.-516_-515delinsCT
XM_017012280.2:c.-513_-512delinsCT	XP_016867769.1:n.-513_-512delinsCT
XM_017012281.2:c.-539_-538delinsCT	XP_016867770.1:n.-539_-538delinsCT
XM_024446786.1:c.66_67delinsCT	XP_024302554.1:p.Pro22=
XM_024446787.1:c.-552_-551delinsCT	XP_024302555.1:n.-552_-551delinsCT
XM_024446788.1:c.-552_-551delinsCT	XP_024302556.1:n.-552_-551delinsCT
XM_024446789.1:c.-552_-551delinsCT	XP_024302557.1:n.-552_-551delinsCT
NM_016203.4:c.198_199delinsCT MANE Select	NP_057287.2:p.Pro66=
NM_001040633.2:c.66_67delinsCT	NP_001035723.1:p.Pro22=