Canonical Allele Identifier: CA1141581464

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237648523G= , CM000663.2:g.237648523G=	GRCh38
NC_000001.10:g.237811823G= , CM000663.1:g.237811823G=	GRCh37
NC_000001.9:g.235878446G=	NCBI36
NG_008799.2:g.611122G=
NG_008799.3:g.611340G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.7422G= MANE Select	NP_001026.2:p.Arg2474=
ENST00000366574.7:c.7422G= MANE Select	ENSP00000355533.2:p.Arg2474=
NM_001035.2:c.7422G=	NP_001026.2:p.Arg2474=
ENST00000360064.7:c.7374G=	ENSP00000353174.7:p.Arg2458=
ENST00000366574.6:c.7422G=	ENSP00000355533.2:p.Arg2474=
ENST00000609119.2:c.7422G=	ENSP00000499659.2:p.Arg2474=
ENST00000659194.3:c.7422G=	ENSP00000499653.3:p.Arg2474=
ENST00000660292.2:c.7422G=	ENSP00000499787.2:p.Arg2474=
XM_006711802.2:c.7452G=	XP_006711865.1:p.Arg2484=
XM_006711802.3:c.7452G=	XP_006711865.1:p.Arg2484=
XM_006711803.2:c.7449G=	XP_006711866.1:p.Arg2483=
XM_006711803.3:c.7449G=	XP_006711866.1:p.Arg2483=
XM_006711804.2:c.7452G=	XP_006711867.1:p.Arg2484=
XM_006711804.3:c.7452G=	XP_006711867.1:p.Arg2484=
XM_006711805.2:c.7422G=	XP_006711868.1:p.Arg2474=
XM_006711805.3:c.7422G=	XP_006711868.1:p.Arg2474=
XM_006711806.2:c.7452G=	XP_006711869.1:p.Arg2484=
XM_006711806.3:c.7452G=	XP_006711869.1:p.Arg2484=
XM_006711807.2:c.7452G=	XP_006711870.1:p.Arg2484=
XM_006711807.3:c.7452G=	XP_006711870.1:p.Arg2484=
XM_006711808.2:c.7452G=	XP_006711871.1:p.Arg2484=
XM_006711808.3:c.7452G=	XP_006711871.1:p.Arg2484=
XM_006711809.2:c.7452G=	XP_006711872.1:p.Arg2484=
XM_006711810.2:c.7419G=	XP_006711873.1:p.Arg2473=
XM_006711810.3:c.7419G=	XP_006711873.1:p.Arg2473=
XM_017002028.1:c.7431G=	XP_016857517.1:p.Arg2477=
XR_002957299.1:n.7766G=
XR_949152.1:n.7733G=
XR_949152.2:n.7766G=