Canonical Allele Identifier: CA345396790

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237640982C>T , CM000663.2:g.237640982C>T	GRCh38
NC_000001.10:g.237804282C>T , CM000663.1:g.237804282C>T	GRCh37
NC_000001.9:g.235870905C>T	NCBI36
NG_008799.2:g.603581C>T
NG_008799.3:g.603799C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.7201C>T MANE Select	NP_001026.2:p.Arg2401Cys
ENST00000366574.7:c.7201C>T MANE Select	ENSP00000355533.2:p.Arg2401Cys
NM_001035.2:c.7201C>T	NP_001026.2:p.Arg2401Cys
ENST00000360064.7:c.7153C>T	ENSP00000353174.7:p.Arg2385Cys
ENST00000366574.6:c.7201C>T	ENSP00000355533.2:p.Arg2401Cys
ENST00000609119.2:c.7201C>T	ENSP00000499659.2:p.Arg2401Cys
ENST00000659194.3:c.7201C>T	ENSP00000499653.3:p.Arg2401Cys
ENST00000660292.2:c.7201C>T	ENSP00000499787.2:p.Arg2401Cys
XM_006711802.2:c.7231C>T	XP_006711865.1:p.Arg2411Cys
XM_006711802.3:c.7231C>T	XP_006711865.1:p.Arg2411Cys
XM_006711803.2:c.7228C>T	XP_006711866.1:p.Arg2410Cys
XM_006711803.3:c.7228C>T	XP_006711866.1:p.Arg2410Cys
XM_006711804.2:c.7231C>T	XP_006711867.1:p.Arg2411Cys
XM_006711804.3:c.7231C>T	XP_006711867.1:p.Arg2411Cys
XM_006711805.2:c.7201C>T	XP_006711868.1:p.Arg2401Cys
XM_006711805.3:c.7201C>T	XP_006711868.1:p.Arg2401Cys
XM_006711806.2:c.7231C>T	XP_006711869.1:p.Arg2411Cys
XM_006711806.3:c.7231C>T	XP_006711869.1:p.Arg2411Cys
XM_006711807.2:c.7231C>T	XP_006711870.1:p.Arg2411Cys
XM_006711807.3:c.7231C>T	XP_006711870.1:p.Arg2411Cys
XM_006711808.2:c.7231C>T	XP_006711871.1:p.Arg2411Cys
XM_006711808.3:c.7231C>T	XP_006711871.1:p.Arg2411Cys
XM_006711809.2:c.7231C>T	XP_006711872.1:p.Arg2411Cys
XM_006711810.2:c.7198C>T	XP_006711873.1:p.Arg2400Cys
XM_006711810.3:c.7198C>T	XP_006711873.1:p.Arg2400Cys
XM_017002028.1:c.7210C>T	XP_016857517.1:p.Arg2404Cys
XR_002957299.1:n.7545C>T
XR_949152.1:n.7512C>T
XR_949152.2:n.7545C>T