Canonical Allele Identifier: CA578748157

Gene: PRKAG2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151869086_151869087insAG , CM000669.2:g.151869086_151869087insAG	GRCh38
NC_000007.13:g.151566171_151566172insAG , CM000669.1:g.151566171_151566172insAG	GRCh37
NC_000007.12:g.151197104_151197105insAG	NCBI36
NG_007486.1:g.13145_13146insCT
NG_007486.2:g.13145_13146insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652321.2:c.114+7420_114+7421insCT	ENSP00000498886.2:n.114+7420_114+7421insCT
ENST00000287878.9:c.114+7420_114+7421insCT MANE Select	ENSP00000287878.3:n.114+7420_114+7421insCT
ENST00000652321.1:c.114+7420_114+7421insCT	ENSP00000498886.1:n.114+7420_114+7421insCT
ENST00000287878.8:c.114+7420_114+7421insCT	ENSP00000287878.3:n.114+7420_114+7421insCT
ENST00000474383.1:n.282+7420_282+7421insCT
ENST00000481434.5:n.619+7420_619+7421insCT
ENST00000488258.5:c.114+7420_114+7421insCT	ENSP00000420783.1:n.114+7420_114+7421insCT
NM_016203.3:c.114+7420_114+7421insCT	NP_057287.2:n.114+7420_114+7421insCT
XM_005250002.2:c.114+7420_114+7421insCT	XP_005250059.1:n.114+7420_114+7421insCT
XM_011516287.1:c.-600+7420_-600+7421insCT	XP_011514589.1:n.-600+7420_-600+7421insCT
XM_005250002.4:c.114+7420_114+7421insCT	XP_005250059.1:n.114+7420_114+7421insCT
XM_017012269.1:c.114+7420_114+7421insCT	XP_016867758.1:n.114+7420_114+7421insCT
XM_017012278.1:c.-600+7420_-600+7421insCT	XP_016867767.1:n.-600+7420_-600+7421insCT
NM_016203.4:c.114+7420_114+7421insCT MANE Select	NP_057287.2:n.114+7420_114+7421insCT