Canonical Allele Identifier: CA370186596

Gene: PRKAG2

Linked Data

• ClinVar Variation Id: 923590
• ClinVar RCV Id: RCV001184415 ; RCV002365869
• dbSNP Id: rs1457532924
• gnomAD v2: 7-151372505-C-T
• gnomAD v4: 7-151675419-C-T
• COSMIC: COSM5573203 ; COSM5573204
• MyVariant Identifiers: chr7:g.151372505C>T (hg19) ; chr7:g.151675419C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151675419C>T , CM000669.2:g.151675419C>T	GRCh38
NC_000007.13:g.151372505C>T , CM000669.1:g.151372505C>T	GRCh37
NC_000007.12:g.151003438C>T	NCBI36
NG_007486.1:g.206812G>A
NG_007486.2:g.206813G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000652321.2:c.684+1G>A	ENSP00000498886.2:n.684+1G>A
ENST00000287878.9:c.684+1G>A MANE Select	ENSP00000287878.3:n.684+1G>A
ENST00000487375.2:n.561+1G>A
ENST00000492843.6:c.312+1G>A	ENSP00000419577.2:n.312+1G>A
ENST00000650858.1:c.-30+1G>A	ENSP00000498384.1:n.-30+1G>A
ENST00000650948.1:n.799+1G>A
ENST00000651188.1:c.552+1G>A	ENSP00000498557.1:n.552+1G>A
ENST00000651303.1:c.552+1G>A	ENSP00000498428.1:n.552+1G>A
ENST00000651378.1:c.-40+1G>A	ENSP00000499103.1:n.-40+1G>A
ENST00000651764.1:c.552+1G>A	ENSP00000498796.1:n.552+1G>A
ENST00000651836.1:c.455+1G>A	ENSP00000499156.1:n.455+1G>A
ENST00000652047.1:c.552+1G>A	ENSP00000499111.1:n.552+1G>A
ENST00000652136.1:n.420+1G>A
ENST00000652159.1:c.552+1G>A	ENSP00000499025.1:n.552+1G>A
ENST00000652321.1:c.684+1G>A	ENSP00000498886.1:n.684+1G>A
ENST00000652707.1:c.552+1G>A	ENSP00000498954.1:n.552+1G>A
ENST00000287878.8:c.684+1G>A	ENSP00000287878.3:n.684+1G>A
ENST00000392801.6:c.552+1G>A	ENSP00000376549.2:n.552+1G>A
ENST00000481434.5:n.1190G>A
ENST00000487375.1:n.562G>A
ENST00000488258.5:c.684+1G>A	ENSP00000420783.1:n.684+1G>A
ENST00000492843.5:c.312+1G>A	ENSP00000419577.1:n.312+1G>A
NM_001040633.1:c.552+1G>A	NP_001035723.1:n.552+1G>A
NM_001304527.1:c.312+1G>A	NP_001291456.1:n.312+1G>A
NM_016203.3:c.684+1G>A	NP_057287.2:n.684+1G>A
XM_005250002.2:c.684+1G>A	XP_005250059.1:n.684+1G>A
XM_005250004.2:c.552+1G>A	XP_005250061.1:n.552+1G>A
XM_005250006.3:c.312+1G>A	XP_005250063.1:n.312+1G>A
XM_006716021.2:c.672+1G>A	XP_006716084.1:n.672+1G>A
XM_011516282.1:c.672+1G>A	XP_011514584.1:n.672+1G>A
XM_011516283.1:c.672+1G>A	XP_011514585.1:n.672+1G>A
XM_011516284.1:c.672+1G>A	XP_011514586.1:n.672+1G>A
XM_011516287.1:c.-30+1G>A	XP_011514589.1:n.-30+1G>A
NM_001363698.1:c.312+1G>A	NP_001350627.1:n.312+1G>A
XM_005250002.4:c.684+1G>A	XP_005250059.1:n.684+1G>A
XM_005250004.4:c.552+1G>A	XP_005250061.1:n.552+1G>A
XM_005250006.5:c.312+1G>A	XP_005250063.1:n.312+1G>A
XM_017012268.2:c.552+1G>A	XP_016867757.1:n.552+1G>A
XM_017012269.1:c.684+1G>A	XP_016867758.1:n.684+1G>A
XM_017012270.1:c.552+1G>A	XP_016867759.1:n.552+1G>A
XM_017012271.2:c.552+1G>A	XP_016867760.1:n.552+1G>A
XM_017012272.1:c.552+1G>A	XP_016867761.1:n.552+1G>A
XM_017012275.2:c.-27+1G>A	XP_016867764.1:n.-27+1G>A
XM_017012276.2:c.-40+1G>A	XP_016867765.1:n.-40+1G>A
XM_017012278.1:c.-30+1G>A	XP_016867767.1:n.-30+1G>A
XM_017012279.2:c.-30+1G>A	XP_016867768.1:n.-30+1G>A
XM_017012280.2:c.-27+1G>A	XP_016867769.1:n.-27+1G>A
XM_017012281.2:c.-27+1G>A	XP_016867770.1:n.-27+1G>A
XM_024446786.1:c.552+1G>A	XP_024302554.1:n.552+1G>A
XM_024446787.1:c.-40+1G>A	XP_024302555.1:n.-40+1G>A
XM_024446788.1:c.-40+1G>A	XP_024302556.1:n.-40+1G>A
XM_024446789.1:c.-40+1G>A	XP_024302557.1:n.-40+1G>A
NM_016203.4:c.684+1G>A MANE Select	NP_057287.2:n.684+1G>A
NM_001040633.2:c.552+1G>A	NP_001035723.1:n.552+1G>A
NM_001304527.2:c.312+1G>A	NP_001291456.1:n.312+1G>A
NM_001363698.2:c.312+1G>A	NP_001350627.1:n.312+1G>A