Canonical Allele Identifier: CA056523

Gene: PRKAG2

Linked Data

• dbSNP Id: rs765005638
• ExAC: 7:151478464 GCCTCTGGAGAAGAAC / G
• gnomAD v2: 7-151478464-GCCTCTGGAGAAGAAC-G
• MyVariant Identifiers: chr7:g.151478465_151478479del (hg19) ; chr7:g.151781379_151781393del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151781382_151781396del , CM000669.2:g.151781382_151781396del	GRCh38
NC_000007.13:g.151478468_151478482del , CM000669.1:g.151478468_151478482del	GRCh37
NC_000007.12:g.151109401_151109415del	NCBI36
NG_007486.1:g.100838_100852del
NG_007486.2:g.100839_100853del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652321.2:c.225_239del	ENSP00000498886.2:p.Phe76_Gly80del
ENST00000287878.9:c.225_239del MANE Select	ENSP00000287878.3:p.Phe76_Gly80del
ENST00000650858.1:c.-248+33023_-248+33037del	ENSP00000498384.1:n.-248+33023_-248+33037del
ENST00000650948.1:n.340_354del
ENST00000651188.1:c.93_107del	ENSP00000498557.1:p.Phe32_Gly36del
ENST00000651303.1:c.93_107del	ENSP00000498428.1:p.Phe32_Gly36del
ENST00000651378.1:c.-258+33023_-258+33037del	ENSP00000499103.1:n.-258+33023_-258+33037del
ENST00000651764.1:c.93_107del	ENSP00000498796.1:p.Phe32_Gly36del
ENST00000652047.1:c.93_107del	ENSP00000499111.1:p.Phe32_Gly36del
ENST00000652159.1:c.93_107del	ENSP00000499025.1:p.Phe32_Gly36del
ENST00000652321.1:c.225_239del	ENSP00000498886.1:p.Phe76_Gly80del
ENST00000652707.1:c.93_107del	ENSP00000498954.1:p.Phe32_Gly36del
ENST00000652714.1:n.398_412del
ENST00000287878.8:c.225_239del	ENSP00000287878.3:p.Phe76_Gly80del
ENST00000392801.6:c.93_107del	ENSP00000376549.2:p.Phe32_Gly36del
ENST00000461529.1:n.244_258del
ENST00000481434.5:n.730_744del
ENST00000488258.5:c.225_239del	ENSP00000420783.1:p.Phe76_Gly80del
NM_001040633.1:c.93_107del	NP_001035723.1:p.Phe32_Gly36del
NM_016203.3:c.225_239del	NP_057287.2:p.Phe76_Gly80del
XM_005250002.2:c.225_239del	XP_005250059.1:p.Phe76_Gly80del
XM_005250004.2:c.93_107del	XP_005250061.1:p.Phe32_Gly36del
XM_006716021.2:c.213_227del	XP_006716084.1:p.Phe72_Gly76del
XM_011516282.1:c.213_227del	XP_011514584.1:p.Phe72_Gly76del
XM_011516283.1:c.213_227del	XP_011514585.1:p.Phe72_Gly76del
XM_011516284.1:c.213_227del	XP_011514586.1:p.Phe72_Gly76del
XM_011516287.1:c.-489_-475del	XP_011514589.1:n.-489_-475del
XM_005250002.4:c.225_239del	XP_005250059.1:p.Phe76_Gly80del
XM_005250004.4:c.93_107del	XP_005250061.1:p.Phe32_Gly36del
XM_017012268.2:c.93_107del	XP_016867757.1:p.Phe32_Gly36del
XM_017012269.1:c.225_239del	XP_016867758.1:p.Phe76_Gly80del
XM_017012270.1:c.93_107del	XP_016867759.1:p.Phe32_Gly36del
XM_017012271.2:c.93_107del	XP_016867760.1:p.Phe32_Gly36del
XM_017012272.1:c.93_107del	XP_016867761.1:p.Phe32_Gly36del
XM_017012275.2:c.-486_-472del	XP_016867764.1:n.-486_-472del
XM_017012276.2:c.-525_-511del	XP_016867765.1:n.-525_-511del
XM_017012278.1:c.-489_-475del	XP_016867767.1:n.-489_-475del
XM_017012279.2:c.-489_-475del	XP_016867768.1:n.-489_-475del
XM_017012280.2:c.-486_-472del	XP_016867769.1:n.-486_-472del
XM_017012281.2:c.-512_-498del	XP_016867770.1:n.-512_-498del
XM_024446786.1:c.93_107del	XP_024302554.1:p.Phe32_Gly36del
XM_024446787.1:c.-525_-511del	XP_024302555.1:n.-525_-511del
XM_024446788.1:c.-525_-511del	XP_024302556.1:n.-525_-511del
XM_024446789.1:c.-525_-511del	XP_024302557.1:n.-525_-511del
NM_016203.4:c.225_239del MANE Select	NP_057287.2:p.Phe76_Gly80del
NM_001040633.2:c.93_107del	NP_001035723.1:p.Phe32_Gly36del