Canonical Allele Identifier: CA2487482391

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784116G= , CM000663.2:g.237784116G=	GRCh38
NC_000001.10:g.237947416G= , CM000663.1:g.237947416G=	GRCh37
NC_000001.9:g.236014039G=	NCBI36
NG_008799.2:g.746715G=
NG_008799.3:g.746933G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3496G=	ENSP00000499659.2:n.*3496G=
ENST00000659194.3:c.12392G=	ENSP00000499653.3:p.Arg4131=
ENST00000660292.2:c.12425G=	ENSP00000499787.2:p.Arg4142=
ENST00000659194.2:c.4581G=
ENST00000366574.7:c.12404G= MANE Select	ENSP00000355533.2:p.Arg4135=
ENST00000659194.1:c.4581G=
ENST00000660292.1:c.2457G=
ENST00000360064.7:c.12356G=	ENSP00000353174.7:p.Arg4119=
ENST00000366574.6:c.12404G=	ENSP00000355533.2:p.Arg4135=
ENST00000609119.1:n.3599G=
NM_001035.2:c.12404G=	NP_001026.2:p.Arg4135=
XM_006711802.2:c.12458G=	XP_006711865.1:p.Arg4153=
XM_006711803.2:c.12455G=	XP_006711866.1:p.Arg4152=
XM_006711804.2:c.12434G=	XP_006711867.1:p.Arg4145=
XM_006711805.2:c.12428G=	XP_006711868.1:p.Arg4143=
XM_006711806.2:c.12422G=	XP_006711869.1:p.Arg4141=
XM_006711807.2:c.12398G=	XP_006711870.1:p.Arg4133=
XM_006711808.2:c.12221G=	XP_006711871.1:p.Arg4074=
XM_006711810.2:c.12365G=	XP_006711873.1:p.Arg4122=
XM_006711802.3:c.12458G=	XP_006711865.1:p.Arg4153=
XM_006711803.3:c.12455G=	XP_006711866.1:p.Arg4152=
XM_006711804.3:c.12434G=	XP_006711867.1:p.Arg4145=
XM_006711805.3:c.12428G=	XP_006711868.1:p.Arg4143=
XM_006711806.3:c.12422G=	XP_006711869.1:p.Arg4141=
XM_006711807.3:c.12398G=	XP_006711870.1:p.Arg4133=
XM_006711808.3:c.12221G=	XP_006711871.1:p.Arg4074=
XM_006711810.3:c.12365G=	XP_006711873.1:p.Arg4122=
XM_017002028.1:c.12437G=	XP_016857517.1:p.Arg4146=
NM_001035.3:c.12404G= MANE Select	NP_001026.2:p.Arg4135=