Canonical Allele Identifier: CA2487482443

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784247G= , CM000663.2:g.237784247G=	GRCh38
NC_000001.10:g.237947547G= , CM000663.1:g.237947547G=	GRCh37
NC_000001.9:g.236014170G=	NCBI36
NG_008799.2:g.746846G=
NG_008799.3:g.747064G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3627G=	ENSP00000499659.2:n.*3627G=
ENST00000659194.3:c.12523G=	ENSP00000499653.3:p.Glu4175=
ENST00000660292.2:c.12556G=	ENSP00000499787.2:p.Glu4186=
ENST00000659194.2:c.4712G=
ENST00000366574.7:c.12535G= MANE Select	ENSP00000355533.2:p.Glu4179=
ENST00000659194.1:c.4712G=
ENST00000660292.1:c.2588G=
ENST00000360064.7:c.12487G=	ENSP00000353174.7:p.Glu4163=
ENST00000366574.6:c.12535G=	ENSP00000355533.2:p.Glu4179=
ENST00000609119.1:n.3730G=
NM_001035.2:c.12535G=	NP_001026.2:p.Glu4179=
XM_006711802.2:c.12589G=	XP_006711865.1:p.Glu4197=
XM_006711803.2:c.12586G=	XP_006711866.1:p.Glu4196=
XM_006711804.2:c.12565G=	XP_006711867.1:p.Glu4189=
XM_006711805.2:c.12559G=	XP_006711868.1:p.Glu4187=
XM_006711806.2:c.12553G=	XP_006711869.1:p.Glu4185=
XM_006711807.2:c.12529G=	XP_006711870.1:p.Glu4177=
XM_006711808.2:c.12352G=	XP_006711871.1:p.Glu4118=
XM_006711810.2:c.12496G=	XP_006711873.1:p.Glu4166=
XM_006711802.3:c.12589G=	XP_006711865.1:p.Glu4197=
XM_006711803.3:c.12586G=	XP_006711866.1:p.Glu4196=
XM_006711804.3:c.12565G=	XP_006711867.1:p.Glu4189=
XM_006711805.3:c.12559G=	XP_006711868.1:p.Glu4187=
XM_006711806.3:c.12553G=	XP_006711869.1:p.Glu4185=
XM_006711807.3:c.12529G=	XP_006711870.1:p.Glu4177=
XM_006711808.3:c.12352G=	XP_006711871.1:p.Glu4118=
XM_006711810.3:c.12496G=	XP_006711873.1:p.Glu4166=
XM_017002028.1:c.12568G=	XP_016857517.1:p.Glu4190=
NM_001035.3:c.12535G= MANE Select	NP_001026.2:p.Glu4179=