Canonical Allele Identifier: CA1752867914

Gene: PRKAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151849504T= , CM000669.2:g.151849504T=	GRCh38
NC_000007.13:g.151546589T= , CM000669.1:g.151546589T=	GRCh37
NC_000007.12:g.151177522T=	NCBI36
NG_007486.1:g.32728A=
NG_007486.2:g.32728A=

Transcript Alleles

HGVS	Amino-acid Change
NM_016203.4:c.114+27003A= MANE Select	NP_057287.2:n.114+27003A=
ENST00000287878.9:c.114+27003A= MANE Select	ENSP00000287878.3:n.114+27003A=
NM_016203.3:c.114+27003A=	NP_057287.2:n.114+27003A=
ENST00000287878.8:c.114+27003A=	ENSP00000287878.3:n.114+27003A=
ENST00000474383.1:n.283-12009A=
ENST00000481434.5:n.619+27003A=
ENST00000488258.5:c.114+27003A=	ENSP00000420783.1:n.114+27003A=
ENST00000652321.1:c.114+27003A=	ENSP00000498886.1:n.114+27003A=
ENST00000652321.2:c.114+27003A=	ENSP00000498886.2:n.114+27003A=
XM_005250002.2:c.114+27003A=	XP_005250059.1:n.114+27003A=
XM_005250002.4:c.114+27003A=	XP_005250059.1:n.114+27003A=
XM_011516287.1:c.-600+27003A=	XP_011514589.1:n.-600+27003A=
XM_017012269.1:c.114+27003A=	XP_016867758.1:n.114+27003A=
XM_017012278.1:c.-600+27003A=	XP_016867767.1:n.-600+27003A=