Canonical Allele Identifier: CA086601

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237593587C>T , CM000663.2:g.237593587C>T	GRCh38
NC_000001.10:g.237756887C>T , CM000663.1:g.237756887C>T	GRCh37
NC_000001.9:g.235823510C>T	NCBI36
NG_008799.2:g.556186C>T
NG_008799.3:g.556404C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.4387C>T MANE Select	NP_001026.2:p.Arg1463Cys
ENST00000366574.7:c.4387C>T MANE Select	ENSP00000355533.2:p.Arg1463Cys
NM_001035.2:c.4387C>T	NP_001026.2:p.Arg1463Cys
ENST00000360064.7:c.4339C>T	ENSP00000353174.7:p.Arg1447Cys
ENST00000366574.6:c.4387C>T	ENSP00000355533.2:p.Arg1463Cys
ENST00000609119.2:c.4387C>T	ENSP00000499659.2:p.Arg1463Cys
ENST00000659194.3:c.4387C>T	ENSP00000499653.3:p.Arg1463Cys
ENST00000660292.2:c.4387C>T	ENSP00000499787.2:p.Arg1463Cys
XM_006711802.2:c.4387C>T	XP_006711865.1:p.Arg1463Cys
XM_006711802.3:c.4387C>T	XP_006711865.1:p.Arg1463Cys
XM_006711803.2:c.4384C>T	XP_006711866.1:p.Arg1462Cys
XM_006711803.3:c.4384C>T	XP_006711866.1:p.Arg1462Cys
XM_006711804.2:c.4387C>T	XP_006711867.1:p.Arg1463Cys
XM_006711804.3:c.4387C>T	XP_006711867.1:p.Arg1463Cys
XM_006711805.2:c.4387C>T	XP_006711868.1:p.Arg1463Cys
XM_006711805.3:c.4387C>T	XP_006711868.1:p.Arg1463Cys
XM_006711806.2:c.4387C>T	XP_006711869.1:p.Arg1463Cys
XM_006711806.3:c.4387C>T	XP_006711869.1:p.Arg1463Cys
XM_006711807.2:c.4387C>T	XP_006711870.1:p.Arg1463Cys
XM_006711807.3:c.4387C>T	XP_006711870.1:p.Arg1463Cys
XM_006711808.2:c.4387C>T	XP_006711871.1:p.Arg1463Cys
XM_006711808.3:c.4387C>T	XP_006711871.1:p.Arg1463Cys
XM_006711809.2:c.4387C>T	XP_006711872.1:p.Arg1463Cys
XM_006711810.2:c.4384C>T	XP_006711873.1:p.Arg1462Cys
XM_006711810.3:c.4384C>T	XP_006711873.1:p.Arg1462Cys
XM_017002028.1:c.4366C>T	XP_016857517.1:p.Arg1456Cys
XR_002957299.1:n.4701C>T
XR_949152.1:n.4668C>T
XR_949152.2:n.4701C>T